| i-bl-iii-bl | Proceedings of the 13th International Symposium on Purine and Pyrimidine Metabolism in Man | S. Eriksson; G. J. Peters |
| i-xi | Purine and Pyrimidine Metabolism in the Fist Decade of the 21st Century—Highlights and Perspectives | Staffan Eriksson; Godefridus J. Peters |
| xii-xvii | In Memoriam: Dr. Hermione Anne Simmonds December 6, 1927 –April 2, 2010 | David Perrett |
| 267-277 | Novel Strategies in the Thiopurine Treatment of Inflammatory Bowel Disease | S. Almer |
| 278-283 | How Should Thiopurine Treatment be Monitored?— Methodological Aspects | S. Vikingsson; B. Carlsson; S. Almer; C. Peterson |
| 284-290 | Limited Intra-Individual Variability in Hypoxanthine-Guanine Phosphoribosyl Transferase, Thiopurine S-Methyl Transferase, and Xanthine Oxidase Activity in Inflammatory Bowel Disease Patients During 6-Thioguanine Therapy | D. P. van Asseldonk; N. K. H. de Boer; K. Smid; C. J. Mulder; A. A. van Bodegraven; G. J. Peters |
| 291-294 | Molecular Analysis of Two Enzyme Genes, HPRT1 and PRPS1, Causing X-Linked Inborn Errors of Purine Metabolism | Y. Yamada; K. Yamada; N. Nomura; A. Yamano; R. Kimura; S. Tomida; M. Naiki; N. Wakamatsu |
| 295-300 | Partial HPRT Deficiency Phenotype and Incomplete Splicing Mutation | R. J. Torres; M. G. Garcia; J. G. Puig |
| 301-305 | Methylation Status of HPRT1 Promoter in HPRT Deficiency with Normal Coding Region | M. G. Garcia; R. J. Torres; J. G. Puig |
| 306-313 | Delayed Treatment Effects of Xanthine Oxidase Inhibition on Systolic Overload-Induced Left Ventricular Hypertrophy and Dysfunction | X. Xu; L. Zhao; X. Hu; P. Zhang; J. Wessale; R. Bache; Y. Chen |
| 314-320 | Establishment and Analysis of SLC22A12 (URAT1) Knockout Mouse | M. Hosoyamada; Y. Takiue; H. Morisaki; J. Cheng; M. Ikawa; M. Okabe; T. Morisaki; K. Ichida; T. Hosoya; T. Shibasaki |
| 321-324 | Effects of Three Strong Statins (Atorvastatin, Pitavastatin, and Rosuvastatin) on Serum Uric Acid Levels in Dyslipidemic Patients | N. Ogata; S. Fujimori; Y. Oka; K. Kaneko |
| 325-329 | Metabolic Syndrome Characteristics in Gout Patients | J. M. Fraile; R. J. Torres; Mendieta E. de Miguel; P. Martínez; K. J. Lundelin; J. J. Vázquez; J. G. Puig |
| 330-334 | Uric Acid Metabolism in Patients with Primary Gout and the Metabolic Syndrome | J. M. Fraile; J. G. Puig; Rosa J. Torres; Eugenio de Miguel; Pedro Martínez; J. J. Vázquez |
| 335-346 | Role of Nucleoside Transporters in Nucleoside-Derived Drug Sensitivity | M. Molina-Arcas; M. Pastor-Anglada |
| 347-351 | Thymidine Kinase 1 Deficient Cells Show Increased Survival Rate After UV-Induced DNA Damage | T. Skovgaard; L. J. Rasmussen; B. Munch-Petersen |
| 352-358 | Thymidine Kinase 1 is a Potential Marker for Prognosis and Monitoring the Response to Treatment of Patients with Breast, Lung, and Esophageal Cancer and Non-Hodgkin's Lymphoma | E. He; X. H. Xu; H. Guan; Y. Chen; Z. H. Chen; Z. L. Pan; L. L. Tang; G. Z. Hu; Y. Li; M. Zhang; J. Zhou; S. Eriksson; T. Fornander; S. Skog |
| 359-362 | Pasteurella Multocida Thymidine Kinase 1 Efficiently Activates Pyrimidine Nucleoside Analogs | A. R. Clausen; S.A. L. Al Meani; J. Piškur |
| 363-369 | Enzymatic Regulation of Cytosolic Thymidine Kinase 1 and Mitochondrial Thymidine Kinase 2: A Mini Review | B. Munch-Petersen |
| 370-381 | Deoxynucleoside Salvage Enzymes and Tissue Specific Mitochondrial DNA Depletion | L. Wang |
| 382-385 | Identification and Characterization of Mitochondrial Factors Modulating Thymidine Kinase 2 Activity | R. Sun; S. Eriksson; L. Wang |
| 386-393 | The Activity of the Lipophilic Nucleoside Derivatives Elacytarabine and CP-4126 in a Panel of Tumor Cell Lines Resistant to Nucleoside Analogues | Marit Liland Sandvold; Carlos Galmarini; Finn Myhren; Godefridus Peters |
| 394-399 | Induction of Resistance to the Lipophilic Cytarabine Prodrug Elacytarabine (CP-4055) in CEM Leukemic Cells | A. D. Adema; N. Losekoot; K. Smid; I. Kathmann; F. Myhren; M. L. Sandvold; G. J. Peters |
| 400-403 | Tissue Specific Distribution of Pyrimidine Deoxynucleoside Salvage Enzymes Shed Light on the Mechanism of Mitochondrial DNA Depletion | L. Wang; S. Eriksson |
| 404-407 | Influence of Phosphorylation of THR-3, SER-11, and SER-15 on Deoxycytidine Kinase Activity and Stability | C. Smal; S. Ntamashimikiro; A. Arts; E. Van Den Neste; F. Bontemps |
| 408-413 | Methylation Specific PCR to Characterize Methylation of the Promoter of Deoxycytidine Kinase | G. J. Peters; J. Hodzic; B. Ortega; E. Giovannetti; A. D. Adema; R. Broekhuizen; G. J. Kaspers; I. Hubeek |
| 414-418 | Effect of Clofarabine on Apoptosis and DNA Synthesis in Human Epithelial Colon Cancer Cells | X. Wang; F. Albertioni |
| 419-426 | Study of Apoptosis Induction and Deoxycytidine Kinase/Cytidine Deaminase Modulation in the Synergistic Interaction of a Novel Ceramide Analog and Gemcitabine in Pancreatic Cancer Cells | E. Giovannetti; L. G. Leon; S. Bertini; M. Macchia; F. Minutolo; N. Funel; C. Alecci; F. Giancola; R. Danesi; G. J. Peters |
| 427-432 | How to Use the Computing Environment R to Analyze ATP-Induced Ribonucleotide Reductase R1 Hexamerization Data | T. Radivoyevitch |
| 433-437 | Ribosylurea Accumulates in Yeast urc4 Mutants | O. Björnberg; M. Vodnala; V. Domkin; A. Hofer; A. Rasmussen; G. Andersen; J. Piškur |
| 438-444 | Synthesis, Biological Properties and Anti-HIV-1 Activity of New Pyrimidine P1,P2-Dinucleotides | A. Miazga; P. Ziemkowski; M. A. Siwecka; A. Lipniacki; A. Piasek; T. Kulikowski |
| 445-448 | Nucleoside Phosphorylases from Clostridium Perfringens in the Synthesis of 2′,3′-Dideoxyinosine | S. Christoffersen; I. Serra; M. Terreni; J. Piškur |
| 449-452 | Protection of Mouse Heart Against Hypoxic Damage by AMP Deaminase Inhibition | T. Borkowski; E. M. Slominska; C. Orlewska; S. Chlopicki; P. Siondalski; M. H. Yacoub; R. T. Smolenski |
| 453-456 | Cardiac Muscle AMP-Deaminase from a 10-Year-Old Male Heterozygous for the AMPD1 C34T Mutation | I. Rybakowska; S. Bakuła; J. Klimek; R. Milczarek; R. T. Smolenski; K. Kaletha |
| 457-460 | Biological Efficiency of AMP Deaminase Inhibitor: 3-[2-(3-CARBOXY-4-BROMO-5,6,7,8-Tetrahydronaphthyl)Ethyl]-3,6,7,8-Tetrahydroimidazo[4,5]-[1,3]Diazepin-8-OL | T. Borkowski; E. M. Slominska; C. Orlewska; A. H. Y. Yuen; S. Al-Ayoubi; P. Siondalski; M. H. Yacoub; R. T. Smolenski |
| 461-465 | Determination of Adenosine Deaminase Activity in Dried Blood Spots by a Nonradiochemical Assay Using Reversed-Phase High-Performance Liquid Chromatography | A. B. P. van Kuilenburg; L. Zoetekouw; J. Meijer; T. W. Kuijpers |
| 466-470 | Identification of Purine Nucleoside Phosphorylase Deficiency in Dried Blood Spots by a Non-Radiochemical Assay Using Reversed-Phase High-Performance Liquid Chromatography | A. B. P. van Kuilenburg; L. Zoetekouw; J. Meijer; T. W. Kuijpers |
| 471-475 | PARP Activity and NAD Concentration in PMC from Patients Affected by Systemic Sclerosis and Lupus Erythematosus | B. Cerboni; A. Di Stefano; V. Micheli; G. Morozzi; G. Pompucci; S. Sestini |
| 476-481 | Region-Specific Distribution of Dihydroorotate Dehydrogenase in the Rat Central Nervous System Points to Pyrimidine De Novo Synthesis in Neurons | Ch. M. Schaefer; M. K. -H. Schäfer; M. Löffler |
| 482-487 | Increased Migration by Stimulation of Thymidine Phosphorylase in Endothelial Cells of Different Origin | I. V. Bijnsdorp; K. Vrijland; L. Vroling; M. Fukushima; G. J. Peters |
| 488-503 | Activation of Stat1, IRF-1, and NF-κB is Required for the Induction of Uridine Phosphorylase by Tumor Necrosis Factor-α and Interferon-γ | Laxiang Wan; Deliang Cao; Jianmin Zeng; Amy Ziemba; Giuseppe Pizzorno |
| 504-508 | Relationship Between Plasma Uridine and Insulin Resistance in Patients with Non-Insulin-Dependent Diabetes Mellitus | Tetsuya Yamamoto; Taku Inokuchi; Tuneyoshi Ka; Asako Yamamoto; Sumio Takahashi; Zenta Tsutsumi; Daisuke Tamada; Chiharu Okuda; Yuji Moriwaki |
| 509-514 | Dihydropyrimidine Dehydrogenase Deficiency Caused by a Novel Genomic Deletion c.505_513del of DPYD | A. B. P. van Kuilenburg; J. Meijer; G. Gökcay; T. Baykal; M. E. Rubio-Gozalbo; A. N. P. M. Mul; C. E. M. de Die-Smulders; P. Weber; A. Capone Mori; J. Bierau; B. Fowler; K. Macke; J. O. Sass; R. Meinsma; J. B. Hennermann; P. Miny; L. Zoetekouw; J. Roelofsen; R. Vijzelaar; J. Nicolai; R. C. M. Hennekam |
| 515-517 | Development of LC-MS Method for Detection of Mutant Uromodulin Protein | M. Yasuda; K. Kaneko; H. Hachisu; M. Ochiai; T. Yamanobe; K. Mawatari; K. Nakagomi; N. Minoura; M. Hosoyamada |
| 518-521 | Analysis of Purine in Purine-Rich Cauliflower | N. Yamaoka; K. Kaneko; Y. Kudo; M. Aoki; M. Yasuda; K. Mawatari; K. Nakagomi; Y. Yamada; T. Yamamoto |
| 333-336 | Foreword: Morris J. Robins—Teacher, Mentor, Scientist, Colleague, and Friend | Stanislaw F. Wnuk |
| 337-351 | Synthesis of 3′-O-Phosphonoethyl Nucleosides with an Adenine and a Thymine Base Moiety | Qiuya Huang; Piet Herdewijn |
| 352-378 | Thiophosphate Analogs of c-di-GMP: Impact on Polymorphism | Jianwei Zhao; Elizabeth Veliath; Seho Kim; Barbara L. Gaffney; Roger A. Jones |
| 379-393 | Biodistribution and Imaging of 1-(2-Deoxy-β-D-Ribofuranosyl)-2,4-Difluoro-5-[123/125I]Iodobenzene (dRF[123/125I]IB), A Nonpolar Thymidine-Mimetic Nucleoside, in Rats and Tumor-Bearing Mice | Anke Stahlschmidt; Panteha Khalili; William Sun; Hans-Jürgen Machulla; Edward E. Knaus; Leonard I. Wiebe |
| 394-407 | Antiproliferative and Protein Kinase Binding Activities of Some N6, 5′-bis-ureido 5′-Amino-5′-Deoxyadenosine Derivatives | Matt A. Peterson; Marcelio Oliveira; Michael A. Christiansen |
| 408-423 | Base-Functionalized Carbocyclic Nucleosides: Design, Synthesis, and Mechanism of Antiviral Activity | Vasu Nair; Fan Zhang; Xiaohui Ma; Eric Bonsu |
| 424-434 | Modulation of RNA Metal Binding by Flanking Bases: 15N NMR Evaluation of GC, Tandem GU, and Tandem GA Sites | Weimin Wang; Jianwei Zhao; Qianwei Han; Gang Wang; Gengcheng Yang; Anthony J. Shallop; Jane Liu; Barbara L. Gaffney; Roger A. Jones |
| 435-449 | Synthesis and Antiviral Evaluation of 4′-C-Azidomethyl-β-D-Ribofuranosyl Purine and Pyrimidine Nucleosides | Jean-François Griffon; Audrey Dumas; Richard Storer; Jean-Pierre Sommadossi; Gilles Gosselin |
| 450-463 | Human Nucleoside Transporters: Biomarkers for Response to Nucleoside Drugs | Vijaya L. Damaraju; Michael B. Sawyer; John R. Mackey; James D. Young; Carol E. Cass |
| 464-472 | The “Corey's Reagent,” 3,5-di-tert-butyl-1,2-Benzoquinone, as a Modifying Agent in the Synthesis of Fluorescent and Double-Headed Nucleosides | Victor A. Timoshchuk; Richard I. Hogrefe |
| 473-484 | Evaluation of NAD(H) Analogues as Selective Inhibitors for Trypanosoma Cruzi S-Adenosylhomocysteine Hydrolase | Qing-Shan Li; Sumin Cai; Jianwen Fang; Ronald T. Borchardt; Krzysztof Kuczera; C. Russell Middaugh; Richard L. Schowen |
| 485-503 | The Rationale for Targeting the NAD/NADH Cofactor Binding Site of Parasitic S-Adenosyl-L-Homocysteine Hydrolase for the Design of Anti-Parasitic Drugs | Sumin Cai; Qing-Shan Li; Jianwen Fang; Ronald T. Borchardt; Krzysztof Kuczera; C. Russell Middaugh; Richard L. Schowen |
| 504-518 | A Convergent Approach for the Synthesis of Ara-Neplanocin a Analogues Under Subzero Microwave Assisted Conditions | Marco Radi; Jagadeeshwar R. Rao; Ashok K. Jha; Chung K. Chu |
| 519-536 | Synthesis and Antiviral Activity of Purine 2′,3′-Dideoxy-2′,3′-Difluoro-D-Arabinofuranosyl Nucleosides | Grigorii G. Sivets; Elena N. Kalinichenko; Igor A. Mikhailopulo; Mervi A. Detorio; Tami R. McBrayer; Tony Whitaker; Raymond F. Schinazi |
| 537-549 | Application of Germyldesulfonylation Reactions to the Synthesis of Germanium-Containing Nucleoside Analogues | Stanislaw F. Wnuk; Pablo R. Sacasa; Jorge Restrepo |
| 550-585 | Nucleosides Part LXVI I[1]: Synthesis of 4-Amino-7(8H)Pteridinone-N8-Nucleosides—Structural Analogs of Adenosine | Oliver Jungmann; Wolfgang Pfleiderer |
| 586-600 | The Unabated Synthesis of New Nucleoside Analogues with Antiviral Potential: A Tribute to Morris J. Robins | Erik De Clercq |
| 601-613 | Truncated Fluorocyclopentenyl Pyrimidines as S-Adenosylhomocysteine Hydrolase Inhibitors | Yeon Hee Park; Won Jun Choi; Amol S. Tipnis; Kang Man Lee; Lak Shin Jeong |
| 614-632 | Contrasting Behavior of Conformationally Locked Carbocyclic Nucleosides of Adenosine and Cytidine as Substrates for Deaminases | Victor E. Marquez; Gottfried K. Schroeder; Olaf R. Ludek; Maqbool A. Siddiqui; Abdallah Ezzitouni; Richard Wolfenden |
| 433-438 | Association of Nuclear Membrane Protein Lamin B1 with Necrosis and Apoptosis in Cell Death Induced by 5-Fluoro-2′-Deoxyuridine | Akira Sato; Akiko Hiramoto; Akito Satake; Eriko Miyazaki; Tomoharu Naito; Yusuke Wataya; Hye-Sook Kim |
| 439-448 | Synthesis and Biological Activity of Mustard Derivatives of Thymine | Amel Hadj-Bouazza; Karine Teste; Ludovic Colombeau; Vincent Chaleix; Rachida Zerrouki; Michel Kraemer; Odile Sainte Catherine |
| 449-459 | Synthesis of 2′-([1,2,3]Triazol-1-yl)-2′-deoxyadenosines | Gavin O′Mahony; Sara Svensson; Andreas Sundgren; Morten Grøtli |
| 460-468 | Synthesis and Antitumor Activity of a Heterodinucleotide of BVDU and Gemcitabine | L. Cappellacci; P. Franchetti; P. Vita; R. Petrelli; M. Grifantini |
| 469-483 | Microwave-Assisted Synthesis and Anti-HIV Activity of New Acyclic C-Nucleosides of 3-(D-Ribo-Tetritol-1-yl)-5-Mercapto-1,2,4-Triazoles. Part 1 | Yaseen A. Al-Soud; Najim A. Al-Masoudi; Thilo Schuppler; Erik De Clercq; Christophe Pannecouque |
| 484-494 | Bicyclic Nucleoside Synthesis—A Photochemical Approach | E. Lee-Ruff; D. Wells |
| 495-505 | Inhibitors Interacting with the Magnesium Binding Site of Reverse Transcriptase: Synthesis and Biological Activity Studies of 3′-(Ω-Amino-Acyl) Amino-3′-Deoxy-Thymidine | Thirumani Venkateshwar Goud; Anne-Marie Aubertin; Jean-François Biellmann |
| 506-524 | The Electron Affinities of Deprotonated Adenine, Guanine, Cytosine, Uracil, and Thymine | Edward C. M. Chen; John R. Wiley; Edward S. Chen |
| 525-533 | 7-Deazainosine Derivatives: Synthesis and Characterization of 7- and 7,8-Substituted Pyrrolo [2,3-d]Pyrimidine Ribonucleosides | Nunzia Ciliberti; Elisa Durini; Stefano Manfredini; Silvia Vertuani |
| 534-545 | Tailoring the Peptide-Binding Specificity Of An RNA by Combinations of Specificity-Altering Mutations | Maki Sugaya; Futoshi Nishimura; Akira Katoh; Kazuo Harada |
| 1307-1310 | dabPna: Design, Synthesis, And Dna Binding Studies | Giovanni N. Roviello; Domenica Musumeci; Maria Moccia; Mariangela Castiglione; Roberto Sapio; Margherita Valente; Enrico M. Bucci; Giuseppe Perretta; Carlo Pedone |
| 1311-1313 | 2′,3′-Isopropylidene Group, A Molecular Scaffold to Study the Activity of Adenosine and Adenylate Deaminase on Adenosine Analogues Modified in the Ribose Moiety | Pierangela Ciuffreda; Laura Alessandrini; Enzo Santaniello |
| 1315-1319 | Synthesis of 3H and 13C Labeled Mrna Cap Dinucleotides—Useful Tools for Nmr, Biochemical, and Biological Studies | Jacek Jemielity; Ryszard Stolarski; Edward Darzynkiewicz |
| 1321-1324 | Synthesis of A New Ribose Modified Analogue of Cyclic Inosine Diphosphate Ribose | Giorgia Oliviero; Nicola Borbone; Jussara Amato; Stefano D'Errico; Gennaro Piccialli; Michela Varra; Luciano Mayol |
| 1325-1328 | New Developments of the “Lock-in” Modified cycloSal-d4TMPs | Dalibor Vukadinović-Tenter; Jan Balzarini; Chris Meier |
| 1329-1333 | Solid-Supported Synthesis of 5′-mRNA CAP-4 from Trypanosomatids | Magdalena Lewdorowicz; Jacek Jemielity; Ryszard Kierzek; Michal Shapira; Janusz Stepinski; Edward Darzynkiewicz |
| 1335-1338 | A Pyrimidopyrimidoindole Nucleoside (dCPPI): Photophysical Properties and Thermal Stability of the Modified Dna Duplexes | Masahiro Mizuta; Kohji Seio; Kenichi Miyata; Akihiro Ohkubo; Haruhiko Taguchi; Mitsuo Sekine |
| 1339-1348 | Synthesis of Leishmania Cap-4 Intermediates, Cap-2 and Cap-3 | Magdalena Lewdorowicz; Janusz Stepinski; Ryszard Kierzek; Jacek Jemielity; Joanna Zuberek; Yael Yoffe; Michal Shapira; Ryszard Stolarski; Edward Darzynkiewicz |
| 1349-1352 | Affinity of Dinucleotide Cap Analogues for Human Decapping Scavenger (hDcpS) | Zbigniew M. Darzynkiewicz; Elzbieta Bojarska; Janusz Stepinski; Jacek Jemielity; Marzena Jankowska-Anyszka; Richard E. Davis; Edward Darzynkiewicz |
| 1353-1357 | Evaluation of Different Chemical Strategies for Conjugation of Oligonucleotides to Peptides | Igor A. Kozlov; Peter C. Melnyk; John P. Hachmann; David L. Barker; Michal Lebl; Chanfeng Zhao |
| 1359-1362 | Synthesis and Incorporation of a Simple Acyclic Furan Containing Phosphoramidite | K. Stevens; A. Madder |
| 1363-1367 | Cg Base Pair Recognition Within Dna Triple Helices Using N-Methyl-3H-Pyrrolo[2,3-d]Pyrimidin-2(7H)-One Nucleoside Analogues | Simon R. Gerrard; Natarajan Srinivasan; Keith R. Fox; Tom Brown |
| 1369-1373 | Looking for New Pyrimidine Acyclic Nucleotide Analogues Designed for Phosphorylation by Human Ump-Cmp Kinase | Dimitri Topalis; Hiroki Kumamoto; Julie A. C. Alexandre; Laurence Dugué; Sylvie Pochet; Sabine Berteina-Raboin; Luigi A. Agrofoglio; Dominique Deville-Bonne |
| 1375-1379 | Enantio-Selectivity of Human Nucleoside Monophosphate Kinases | J. A. C. Alexandre; B. Roy; D. Topalis; C. Périgaud; D. Deville-Bonne |
| 1381-1386 | Synthesis of Pyrene Labeled Rna for Fluorescence Measurements | Taewoo Kwon; Nelly Piton; Christian Grünewald; Joachim W. Engels |
| 1387-1389 | Synthesis of 9-(2,3-Dideoxy-2,3-Difluoro-β-D- Arabinofuranosyl)Adenine | Grigorii G. Sivets; Elena N. Kalinichenko; Igor A. Mikhailopulo |
| 1391-1394 | Alkyne-Azide Click Chemistry Mediated Carbanucleosides Synthesis | Julie Broggi; Nicolas Joubert; Vincent Aucagne; Sabine Berteina-Raboin; S. Diez-Gonzalez; Steve Nolan; Dimitri Topalis; Dominique Deville-Bonne; Jan Balzarini; Johan Neyts; Graciela Andrei; Robert Snoeck; Luigi A. Agrofoglio |
| 1395-1398 | Supported Synthesis and Functionnalization of 2″-Deoxyuridine by Suzuki-Miyaura Cross-Coupling | Saïd El Kazzouli; Sabine Berteina-Raboin; Luigi A. Agrofoglio |
| 1399-1402 | Cross-Metathesis Mediated Synthesis of New Acyclic Nucleoside Phosphonates | Vincent Roy; Hiroki Kumamoto; Sabine Berteina-Raboin; Steven P. Nolan; Dimitri Topalis; Dominique Deville-Bonne; Jan Balzarini; Johan Neyts; Gracelia Andrei; Robert Snoeck; Luigi A. Agrofoglio |
| 1403-1405 | Synthesis and Biophysical Studies of N2′-Functionalized 2′-Amino-α-L-LNA | T. Santhosh Kumar; Andreas S. Madsen; Jesper Wengel; Patrick J. Hrdlicka |
| 629-634 | Methylation-Dependent Fragment Separation: Novel Analysis Of 5-Methyl Cytosine By Capillary Electrophoresis Of Amplified Dna Using Pcr Incorporation Of Chemically Modified Dctp | Victoria L. Boyd; Kristina I. Moody; Achim E. Karger; Kenneth J. Livak; Gerald Zon; John W. Burns |
| 635-640 | Discovery of ANA975: An Oral Prodrug of the TLR-7 Agonist Isatoribine | Alan X. Xiang; Stephen E. Webber; Bradley M. Kerr; Erik J. Rueden; Joseph R. Lennox; Gregory J. Haley; Tingmin Wang; John S. Ng; Mark R. Herbert; David L. Clark; Virginia N. Banh; Wei Li; Simon P. Fletcher; Kevin R. Steffy; Darian M. Bartkowski; Leonid I. Kirkovsky; Lisa A. Bauman; Devron R. Averett |
| 641-644 | Aryl-Containing Esters Of Triphosphoric Acid As Substrates Of Terminal Deoxynucleotidyl Transferase | A. L. Khandazhinskaya; E. S. Matyugina; L. A. Alexandrova; E. A. Shirokova; M. K. Kukhanova; M. V. Jasko |
| 645-649 | Selective Fluorescence Detection Of 8-Oxoguanosine With 8-Oxog-Clamp | Osamu Nakagawa; Sayaka Ono; Akira Tsujimoto; Zhichun Li; Shigeki Sasaki |
| 651-654 | Impdh As A Biological Probe For Rna Antiviral Drug Discovery: Synthesis, Enzymology, Molecular Docking, And Antiviral Activity Of New Ribonucleosides With Surrogate Bases | Vasu Nair; Xiaohui Ma; Qingning Shu; Fan Zhang; Vinod Uchil; Govardhan R. Cherukupalli |
| 655-659 | The Synthesis Of Epr Differentiable Spinlabels And Their Coupling To Uridine | Olga Frolow; Bela E. Bode; Joachim W. Engels |
| 661-664 | PNA Conjugated to High-Molecular Weight Poly(Ethylene Glycol): Synthesis and Properties | Gian Maria Bonora; Sara Drioli; Maurizio Ballico; Andrea Faccini; Roberto Corradini; Susanna Cogoi; Luigi Xodo |
| 665-668 | Biologically-Validated HIV Integrase Inhibitors with Nucleobase Scaffolds: Structure, Synthesis, Chemical Biology, Molecular Modeling, and Antiviral Activity | Vasu Nair; Vinod Uchil; Guochen Chi; Iwona Dams; Arthur Cox; Byung Seo |
| 669-674 | Biophysical Properties of Quadruplexes Containing Two or Three 8-Bromodeoxyguanosine Residues | Luigi Petraccone; Ida Duro; Antonio Randazzo; Ada Virno; Luciano Mayol; Concetta Giancola |
| 675-679 | Effect of the Incorporation of 2′-Deoxy-8-(Hydroxyl)Adenosine on the Stability of Quadruplexes Formed by Modified Human Telomeric DNA | Luigi Petraccone; Ida Duro; Eva Erra; Antonio Randazzo; Ada Virno; Concetta Giancola |
| 681-685 | Synthesis of New, Base-Modified PNA Monomers | Ferenc Sipos; Gyula Sági |
| 687-690 | Isonucleosides: Design and Synthesis of New Isomeric Nucleosides with Antiviral Potential | Vasu Nair; Dorota G. Piotrowska; Maurice Okello; Jean Vadakkan |
| 691-694 | Development Of An Antitumor Adenosine Analog, 3″-Ethynyladenosine | Yoshio Endo; Tohru Obata; Makoto Nomura; Masakazu Fukushima; Yuji Yamada; Akira Matsuda; Takuma Sasaki |
| 695-699 | 7,5′-O-Dibenzylinosines: Synthesis and Studies on Their Conformational Properties | Elena Casanova; Leire Aguado; María-Luisa Jimeno; Federico Gago; María-José Camarasa; María-Jesús Pérez-Pérez |
| 701-704 | Transformation of D-(-)-Ribose into a Natural Product-Like Scaffold via a Lewis Acid Catalyzed Intramolecular Hetero-Diels-Alder Reaction | Roland Messer; Cyril A. Fuhrer; Robert Häner |
| 705-708 | Synthesis of DNA-Oligonucleotides Damaged by Arylamine-Modified 2′-Deoxyguanosine | N. Böge; Z. Szombati; C. Meier |
| 709-712 | Synthesis of 3′- S-Phosphorothiolate Oligonucleotides for their Potential Use in RNA Interference | James W. Gaynor; John Brazier; Rick Cosstick |
| 713-716 | Synthesis and Antitumor Activity of Fluorocyclopentenyl-Pyrimidines | Lak Shin Jeong; Long Xuan Zhao; Won Jun Choi; Shantanu Pal; Yeon Hee Park; Sang Kook Lee; Moon Woo Chun; Young B. Lee; Chang Ho Ahn; Hyung Ryong Moon |
| 717-719 | Synthesis of N6-Substituted 3′-Ureidoadenosine Derivatives as Highly Potent Agonists at the Mutant A3 Adenosine Receptor | Lak Shin Jeong; Seung Ah Choe; Ae Yil Kim; Hea Ok Kim; Zhan-Guo Gao; Kenneth A. Jacobson; Moon Woo Chun; Hyung Ryong Moon |
| 721-724 | Asymmetric Synthesis of Novel Apio Carbocyclic Nucleoside Analogues as Potential Antiviral and Antitumor Agent | Lak Shin Jeong; Jeong A. Lee; Hyung Ryong Moon; Hea Ok Kim; Kang Man Lee; Hyun Joo Lee; Moon Woo Chun |
| 1387-1394 | John A. Montgomery, March 29, 1924–May 24, 2004 | Jack Secrist |
| 1395-1415 | John Montgomery's Legacy: Carbocyclic Adenosine Analogues as Sah Hydrolase Inhibitors with Broad-Spectrum Antiviral Activity | E. De Clercq |
| 1417-1437 | Design, Synthesis, and Antiviral Evaluation of Some Polyhalogenated Indole C-nucleosides | Jiong J. Chen; Yuan Wei; John D. Williams; John C. Drach; Leroy B. Townsend |
| 1439-1447 | Reaction of the 2′-Silyl and 2′-Stannyl Derivatives of 6-(Bromomethyl)Dimethylsilyl-1′,2′-Unsaturated Uridine Under Radical Conditions | Junko Ogamino; Hideaki Mizunuma; Hiroki Kumamoto; Kazuhiro Haraguchi; Hiromichi Tanaka |
| 1449-1468 | Synthetic Approaches to Nuclease-Resistant, Nonnatural Dinucleotides of Anti-Hiv Integrase Interest | Guochen Chi; Vasu Nair |
| 1469-1484 | Stereochemistry of Internucleotide Bond Formation by the H-Phosphonate Method. 1. Synthesis and 31P Nmr Analysis of 16 Diribonulceoside (3′-5′)-H-Phosphonates and the Corresponding Phosphorothioates | Michal Sobkowski; Jadwiga Jankowska; Adam Kraszewski; Jacek Stawinski |
| 1485-1505 | Oligonucleotides Containing Pyrazolo[3,4-d]Pyrimidines: 8-Aza-7-deazaadenines With Bulky Substituents in the 2- or 7-Position | Frank Seela; Anup M. Jawalekar; Lijuan Sun; Peter Leonard |
| 1507-1517 | Nucleoside Modification and Concerted Mutagenesis of the Human A3 Adenosine Receptor to Probe Interactions Between the 2-Position of Adenosine Analogs and Gln167 in the Second Extracellular Loop | Heng T. Duong; Zhan-Guo Gao; Kenneth A. Jacobson |
| 1519-1530 | Preference for Ribose Over Deoxyribose in Loop-Closing Base Pairs of Extra Stable Nucleic Acid Hairpins | Rami N. Hannoush; Masad J. Damha |
| 1531-1542 | Synthesis and Anti-Hcv Activity of N9, 5′-Cyclo-3-(β-D-Ribofuranosyl)-8-Azapurin-2-One Derivatives | Abdalla E. A. Hassan; Peiyuan Wang; Tamara McBrayer; Philip Tharnish; Lieven Stuyver; Michael J. Otto; Kyoichi A. Watanabe; Raymond F. Schinazi |
| 1543-1568 | Synthesis of 9-[1-(Substituted)-3-(phosphonomethoxy)propyl]adenine Derivatives as Possible Antiviral Agents | Minwan Wu; Yahya El-Kattan; Tsu-Hsing Lin; Ajit Ghosh; Satish Vadlakonda; Pravin L. Kotian; Yarlagadda S. Babu; Pooran Chand |
| 1569-1585 | Synthesis of 9-[1-(Substituted)-2-(Phosphonomethoxy)Ethyl]Adenine Derivatives as Possible Antiviral Agents | Minwan Wu; Yahya El-Kattan; Tsu-Hsing Lin; Ajit Ghosh; V. Satish Kumar; Pravin L. Kotian; Xiaogang Cheng; Shanta Bantia; Yarlagadda S. Babu; Pooran Chand |
| 1587-1595 | Synthesis of 9-[1-(1-Hydroxyethyl)-3-(Phosphonomethoxy)Propyl] Adenine and Prodrug as Possible Antiviral Agents | Ajit Ghosh; Yahya El-Kattan; Minwan Wu; Tsu-Hsing Lin; Satish Vadlakonda; Pravin L. Kotian; Yarlagadda S. Babu; Pooran Chand |
| 1597-1611 | Synthesis of N6-Substituted 9-[3-(Phosphonomethoxy)Propyl]Adenine Derivatives As Possible Antiviral Agents | Yahya El-Kattan; Tsu-Hsing Lin; Minwan Wu; V. Satish Kumar; Pravin L. Kotian; Ajit Ghosh; Xiaogang Cheng; Shanta Bantia; Yarlagadda S. Babu; Pooran Chand |
| 1613-1626 | Synthesis and Antiviral Activity of Some 2-Substituted 3-Formyl-and 3-Cyano-5,6-Dichloroindole Nucleosides | John D. Williams; John C. Drach; Leroy B. Townsend |
| 1627-1633 | Preparation of Nucleoside H-Phosphonoselenoate Monoesters Via the Phosphinate Approach | Martin Kullberg; Jacek Stawinsk |
| 1635-1649 | Synthetic Approaches to a Mononucleotide Prodrug of Cytarabine | R. Bazzanini; M. -H. Gouy; S. Peyrottes; G. Gosselin; C. Périgaud; S. Manfredini |
| 1651-1664 | 2′,3′-Dideoxynucleoside 5′-β,γ-(Difluoromethylene) Triphosphates With α-P-Thio or α-P-Seleno Modifications: Synthesis and Their Inhibition of HIV-1 Reverse Transcriptase | Nicholas A. Boyle; Patrick Fagan; Jennifer L. Brooks; Marija Prhavc; John Lambert; P. Dan Cook |
| 1665-1706 | Nucleotides. LXXIV Synthesis of a-D-Arabino-oligonucleotides | Christoph Henke; Wolfgang Pfleiderer |
| 1707-1727 | Synthesis and Anti-HIV Activity of β-D-3′-Azido-2′,3′-unsaturated Nucleosides and β-D-3′-Azido-3′-deoxyribofuranosylnucleosides | Srinivas Gadthula; Chung K. Chu; Raymond F. Schinazi |
| 1729-1743 | An Efficient Alternative Route To 3,6-Disubstituted-Furo[2,3-d]Pyrimidin-2-One Analogues | Zlatko Janeba; Noha Maklad; Morris J. Robins |
| 1745-1761 | The Middle to 3′ End of the Hiv-1 Vif Gene Sequence is Important for Vif Biological Activity and Could be Used for Antisense Oligonucleotide Targets | Jacob Samson Barn; Naoko Miyano-Kurosaki; Hiroshi Takaku; Kazuya Yamaguchi; Atsushi Sakamoto; Koichi Ishikawa; Naoki Yamamoto; Mubarak Osei-Kwasi; David Ofori-Adjei |
| 1763-1774 | Phosphoralaninate Pronucleotides of Pyrimidine Methylenecyclopropane Analogues of Nucleosides: Synthesis and Antiviral Activity | Amalraj Ambrose; Jiri Zemlicka; Earl R. Kern; John C. Drach; Elizabeth Gullen; Yung-Chi Cheng |
| 1775-1788 | A Novel Imidazole Nucleoside Containing a Diaminodihydro-S-triazine as a Substituent: Inhibitory Activity Against the West Nile Virus NTPase/Helicase | Ravi K. Ujjinamatada; Yankanagouda S. Agasimundin; Peng Zhang; Ramachandra S. Hosmane; Roman Schuessler; Peter Borowski; Kishna Kalicharran; Ali Fattom |
| 1789-1800 | Nucleosides and Nucleotides. 232. Synthesis of 2′-C-Methyl-4′-thiocytidine: Unexpected Anomerization of the 2′-Keto-4′-thionucleoside Precursor | Daisuke Kaga; Noriaki Minakawa; Akira Matsuda |
| 1801-1815 | Binding of G-Quadruplex-interactive Agents to Distinct G-Quadruplexes Induces Different Biological Effects in MiaPaCa Cells | Weijun Liu; Daekyu Sun; Laurence H. Hurley |
| 1817-1830 | Synthesis and Pharmacokinetic and Pharmacodynamic Evaluation of the Forodesine HCl Analog BCX-3040 | Hollis S. Kezar III; J. Michael Kilpatrick; Deborah Phillips; Debbie Kellogg; Jianwen Zhang; Philip E. Morris Jr. |
| 1831-1842 | Synthesis of a Convenient Thymidine Glycol Phosphoramidite Monomer and Its Site-specific Incorporation into DNA Fragments | Didier Gasparutto; Sonia Cognet; Solveig Roussel; Jean Cadet |
| 1843-1852 | 2′-MeO-RNA Containing Oligodeoxyribonucleotide Primers Can Prevent Template-independent Base Extension on Microarrays | Xiaodong Zhao |
| 1853-1874 | Synthesis and Application of Negatively Charged PNA Analogues | Vladimir A. Efimov; Oksana G. Chakhmakhcheva; Eric Wickstrom |
| 1875-1884 | Confocal-microscopy Studies of a Model Oligoribonucleotide HIV Inhibitor | Robyn M. Hyde; Keith Jensen; Jindrich Kopecek; Arthur D. Broom |
| 1885-1894 | Double-headed Acyclo C-Nucleoside Analogues. Functionalized 1,2-bis-(1,2,4-Triazol-3-yl)ethane-1,2-diol | A. H. Moustafa; R. A. Haggam; M. E. Younes; E. S. H. El Ashry |
| 1895-1906 | Synthesis and Biological Activity of 4′-Thio-L-xylofuranosyl Purine Nucleosides | Kamal N. Tiwari; Lea Messini; John A. Montgomery; John A. Secrist III |
| 1907-1917 | Suppression of Human Immunodeficiency Virus Type 1 (HIV-1) Replication by an HIV-1-dependent Double Locked Vector with the Cre/loxP System | Yuichiro Habu; Takashi Nagawa; Norihiko Matsumoto; Hiroaki Takeuchi; Naoko Miyano-Kurosaki; Hiroshi Takaku |
| 1919-1945 | Synthesis and Structural Analysis of Oxadiazole Carboxamide Deoxyribonucleoside Analogs | Olga Adelfinskaya; Weidong Wu; V. Jo Davisson; Donald E. Bergstrom |
| 1947-1970 | Solid-phase Parallel Synthesis of 4-β-D-Ribofuranosylpyrazolo[4,3-d]pyrimidine Nucleosides | Kanda S. Ramasamy; Roberto B. Amador; Qazi Habib; Frank Rong; Xiaogang Han; David Y. Li; Jingfan Huang; Zhi Hong; Haoyun An |
| 1971-1996 | Synthesis of 3-Aminoimidazo[4,5-c]pyrazole Nucleoside via the N-N Bond Formation Strategy as a [5:5] Fused Analog of Adenosine | Tun-Cheng Chien; David A. Berry; John C. Drach; Leroy B. Townsend |
| 1997-2022 | Pyrimidine and Purine Analogues, Effects on Cell Cycle Regulation and the Role of Cell Cycle Inhibitors to Enhance Their Cytotoxicity | Jennifer Sigmond; Godefridus J. Peters |
| 2023-2027 | Ribose-modified Mizoribine Analogues: Synthesis and Biological Evaluation | Palmarisa Franchetti; Michela Pasqualini; Loredana Cappellacci; Riccardo Petrelli; Patrizia Vita; Mario Grifantini; Hiremagalur N. Jayaram |
| 927-929 | A New Protecting Group for the 5′-Hydroxyl Group Having O–S Single Bond Oxidatively Cleavable Under Mild Conditions | Eri Utagawa; Kohji Seio; Mitsuo Sekine |
| 931-934 | Perylene Attached to DNA Through Stiff or Flexible Linker: Duplex Stability and Fret | Mikhail V. Skorobogatyj; Anna A. Pchelintseva; Alexei V. Ustinov; Vladimir A. Korshun; Andrei D. Malakhov |
| 935-938 | 2-Substituted 5′-N-Methylcarboxamidoadenosine (MECA) Derivatives as A3 Adenosine Receptor Ligands | S. Vittori; R. Volpini; C. Lambertucci; S. Taffi; K. N. Klotz; G. Cristalli |
| 939-942 | "Lock-in" Modified CycloSal Nucleotides—The Second Generation of CycloSal Prodrugs | D. Vukadinović; N. P. H. Böge; J. Balzarini; C. Meier |
| 943-946 | Incorporation of Ribonucleoside 5′-(α-P-Borano)Triphosphates Into a 20-MER RNA by T7 RNA Polymerase | Jing Wan; Barbara Ramsay Shaw |
| 947-950 | Synthesis of 5-(1-Propynyl)-2′-Deoxyuridine 5′-(Alpha-P-Borano)Triphosphate and Kinetic Characterization as a Substrate for MMLV Reverse Transcriptase | Joy Xin Wang; Barbara Ramsay Shaw |
| 951-955 | The Effect of a Single Boranophosphate Substitution with Defined Configuration on the Thermal Stabiltiy and Conformation of a DNA Duplex | Joy Xin Wang; Dmitri S. Sergueev; Barbara Ramsay Shaw |
| 957-960 | Synthesis of N 3,5′-Cyclo-4-(β-d-Ribofuranosyl)-vic-Triazolo[4,5-b]Pyridin-5-One and Its 3′-Deoxysugar Analogue as Potential Anti-Hepatitis C Virus Agents | Peiyuan Wang; Laurent Hollecker; Krzysztof W. Pankiewicz; Steven E. Patterson; Tony Whitaker; Tamara R. McBrayer; Phillip M. Tharnish; Lieven J. Stuyver; Raymond F. Schinazi; Michael J. Otto; Kyoichi A. Watanabe |
| 961-964 | Synthesis and Anti-Hepatitis C Virus Activity of Nucleoside Derivatives of N 3 ,5′-Anhydro-4-(β-d-Ribofuranosyl)-8-Azapurin-2-Ones | Abdalla E. A. Hassan; Peiyuan Wang; Tamara R. McBrayer; Phillip M. Tharnish; Lieven J. Stuyver; Raymond F. Schinazi; Michael J. Otto; Kyoichi A. Watanabe |
| 965-969 | Synthesis and Characterization of DNA Duplexes Containing an N3T-Ethyl-N3T Interstrand Crosslink in Opposite Orientations | Christopher J. Wilds; Anne M. Noronha; Sebastien Robidoux; Paul S. Miller |
| 971-974 | Antigene Property of PNA Conjugated to the Nuclear Localization Signal Peptide | Susanna Cogoi; Andrea Codognotto; Valentina Rapozzi; Luigi E. Xodo |
| 975-977 | Synthesis of 3′-Deoxy-3′-C-Hydroxymethyl Analogues of Tiazofurin and Ribavirin | Moon Woo Chun; Myong Jung Kim; Ji Hye Shin; Lak Shin Jeong |
| 979-981 | Synthesis of Homo-N-Nucleoside with 1,2,4-Triazole-3-Carboxamide | Moon Woo Chun; Jin Hee Kim; Myong Jung Kim; Bo Ram Kim; Lak Shin Jeong |
| 983-987 | Affinity of (α-P-Borano)-NTP Analogs to Rabbit Muscle Pyruvate Kinase | Mikhail I. Dobrikov; Barbara Ramsay Shaw |
| 989-992 | A Novel Amino-ON CPG-Support for the Synthesis of 3′-Aminoalkylated Oligonucleotides | Michael Leuck; Rubina Giare; Nicole Zien; Matthias Paul; Andreas Wolter |
| 993-998 | Enzymatic Resolution and Base Pairing Properties of d - and l -Cyclohexenyl Nucleic Acids (CeNA) | Ping Gu; Guy Schepers; Carsten Griebel; Jef Rozenski; Hans-Joachim Gais; Piet Herdewijn; Arthur Van Aerschot |
| 999-1008 | Photolabeling Probes of Ribavirin and Eicar | Qiongyou Wu; Fanqi Qu; Jinqiao Wan; Yi Xia; Ling Peng |
| 1009-1013 | Silyl Protecting Groups for Oligonucleotide Synthesis Removed by A ZnBr2 Treatment | Fernando Ferreira; François Morvan |
| 1015-1018 | Synthesis of Conformationally Restricted Nucleic Acid Fragments Using Ring-Closing Alkene and Enyne Metathesis Reactions | Signe I. Steffansen; Mikkel S. Christensen; Philip Børsting; Poul Nielsen |
| 1019-1021 | Promotion of Pyrimidine Motif Triplex Formation by Morpholino Modification of Triplex-Forming Oligonucleotide: Kinetic and Thermodynamic Studies | Hidetaka Torigoe; Kouji Kawahashi; Yuusuke Tamura |
| 1023-1027 | RNA Recognition by Fluor-Aromatic Substituted | A. Živković; J. W. Engels |
| 1029-1032 | PROSIT, an Online Service to Calculate Pseudorotational Parameters of Nucleosides and Nucleotides | Guangyu Sun; Johannes H. Voigt; Victor E. Marquez; Marc C. Nicklaus |
| 1033-1036 | A Cautionary Note on the Use of the 31P NMR Spectroscopy in Stereochemical Correlation Analysis | Michal Sobkowski; Jadwiga Jankowska; Jacek Stawinski; Adam Kraszewski |
| 1037-1041 | Significant Improvement of Quality for Long Oligonucleotides by Using Controlled Pore Glass with Large Pores | Igor A. Kozlov; Minh Dang; Ken Sikes; Theofilos Kotseroglou; David L. Barker; Chanfeng Zhao |
| 1043-1046 | Functionalization of Pyrimidine and Purine Nucleosides at C4 and C6: C-Nucleophilic Substitution of Their C4- and C6-(1,2,4-Triazol-1-yl) Derivatives | Victor Timoshchuk |
| 1047-1049 | Synthesis of 5-Ethynyl-2′-Deoxyuridine-5′-Boranomono Phosphate as a Potential Thymidylate Synthase Inhibitor | Shoeb I. Khan; Mikhail I. Dobrikov; Barbara Ramsay Shaw |
| 1051-1054 | Synthetic Study of 3′-α-Fluoro-2′,3′-Dideoxyguanosine | Takayoshi Torii; Tomoyuki Onishi; Shigehisa Tanji; Kunisuke Izawa |
| 1055-1058 | Presence of 2′,5′-Linkages in a Homopyrimidine DNA Oligonucleotide Promotes Stable Triplex Formation Under Physiological Conditions | Satoshi Obika; Akiko Hiroto; Osamu Nakagawa; Takeshi Imanishi |
| 1059-1061 | A Convenient Method for the Synthesis of Oligonucleotide-Cationic Peptide Conjugates | G. Ferenc; Z. Kupihár; Z. Kele; L. Kovács |
| 1063-1067 | A New Approach to Oligonucleotide N3′→P5′ Phosphoramidate Building Blocks | Daria Zielinska; Krisztina Pongracz; Sergei Gryaznov |
| i-ii | List of Contributors | |
| 1815-1824 | Synthesis and Antiviral Properties of Arabino and Ribonucleosides of 1,3-Dideazaadenine, 4-Nitro-1, 3-dideazaadenine and Diketopiperazine | Sarika Sinha; Richa Srivastava; Erik De Clercq; Ramendra K. Singh |
| 1825-1832 | First Synthesis of Double Headed 1,3,4-Oxadiazino[6,5-b]indole Acyclo C-Nucleosides | Adel Z. Nasr |
| 1833-1847 | The Chemical and Biochemical Properties of Methylphosphotriester DNA | Henk M. Buck |
| 1849-1864 | Effective Anomerisation of 2′-Deoxyadenosine Derivatives During Disaccharide Nucleoside Synthesis | Irina V. Gulyaeva; Kari Neuvonen; Harri Lönnberg; Andrei A. Rodionov; Elena V. Shcheveleva; Georgii V. Bobkov; Ekaterina V. Efimtseva; Sergey N. Mikhailov |
| 1865-1874 | Phosphorylation of Isocarbostyril- and Difluorophenyl-Nucleoside Thymidine Mimics by the Human Deoxynucleoside Kinases | Ashraf Said Al-Madhoun; Staffan Eriksson; Zhi-Xian Wang; Ebrahim Naimi; Edward E. Knaus; Leonard I. Wiebe |
| 1875-1887 | Synthesis of (-)-DAPD | Marcos L. Sznaidman; Jinfa Du; Amir Pesyan; Darryl G. Cleary; Kevin P. Hurley; Frank Waligora; Merrick R. Almond |
| 1889-1910 | Synthesis of Some Novel 6-Benzyl(or Substituted Benzyl)-2-β-d-Glucopyranosyl-1,2,4-Triazolo[4,3-b][1,2,4]Triazines as Potential Antimicrobial Chemotherapeutics | Nasser S. A. M. Khalil; Abdel Kader Mansour; Mohga M. Eid |
| 1911-1927 | The Solution Synthesis of Antisense Oligonucleotide-Peptide Conjugates Directly Linked via Phosphoramide Bond by Using a Fragment Coupling Approach | Nataliya V. Sumbatyan; Vassili A. Mandrugin; Alain Deroussent; Jean-Rémi Bertrand; Zsuzsa Majer; Claude Malvy; Galina A. Korshunova; Miklos Hollosi; Marina B. Gottikh |
| 1929-1937 | Phosphoramidate Protides of Carbocyclic 2′,3′-Dideoxy-2′,3′-Didehydro-7-Deazaadenosine with Potent Activity Against HIV and HBV | Kristjan S. Gudmundsson; Zhicheng Wang; Susan M. Daluge; Lance C. Johnson; Richard Hazen; Lynn D. Condreay; Christopher McGuigan |
| 1077-1079 | Purine and Pyrimidine Metabolism: New Challenges | G. J. Peters; A. B. P. van Kuilenburg; R. A. de Abreu |
| 1081-1082 | Dedication to Francoise Roch-Ramel | H. A. Simmonds |
| 1083-1088 | Antimetabolites in the Treatment of Arthritis: Current Status of the Use of Antimetabolites | B. A. C. Dijkmans; G. Jansen |
| 1089-1100 | Two Inhibitors of DNA-Synthesis Lead to Inhibition of Cytokine Production via a Different Mechanism | S. de Lathouder; A. H. Gerards; B. A. C. Dijkmans; L. A. Aarden |
| 1101-1106 | Modification of Cytokine Milieu by A2A Adenosine Receptor Signaling–Possible Application for Inflammatory Diseases | M. Koshiba; Y. Nakamachi; H. Kosaka; T. Nakazawa; G. Tsuji; S. Kumagai |
| 1107-1110 | Purine Modulation of Cytokine Release During Diuretic Therapy of Rheumatoid Arthritis | C. M. Forrest; G. Harman; R. B. McMillan; C. Rana; S. Shaw; T. W. Stone; N. Stoy; L. G. Darlington |
| 1111-1116 | Febuxostat (TMX-67), a Novel, Non-Purine, Selective Inhibitor of Xanthine Oxidase, Is Safe and Decreases Serum Urate in Healthy Volunteers | M. A. Becker; J. Kisicki; R. Khosravan; J. Wu; D. Mulford; B. Hunt; P. MacDonald; N. Joseph-Ridge |
| 1117-1118 | PK/PD and Safety of a Single Dose of TMX-67 (Febuxostat) in Subjects with Mild and Moderate Renal Impairment | S. Hoshide; Y. Takahashi; T. Ishikawa; J. Kubo; M. Tsuchimoto; K. Komoriya; I. Ohno; T. Hosoya |
| 1119-1122 | Pharmacokinetics and Pharmacodynamics of Febuxostat (TMX-67), a Non-Purine Selective Inhibitor of Xanthine Oxidase/Xanthine Dehydrogenase (NPSIXO) in Patients with Gout and/or Hyperuricemia | K. Komoriya; S. Hoshide; K. Takeda; H. Kobayashi; J. Kubo; M. Tsuchimoto; T. Nakachi; H. Yamanaka; N. Kamatani |
| 1123-1125 | Pharmacokinetics/Pharmacodynamics of Y-700, A Novel Xanthine Oxidase Inhibitor, in Rats and Man | I. Yamada; A. Fukunari; T. Osajima; M. Kamezawa; H. Mori; J. Iwane |
| 1127-1129 | Detection of Prothrombin and Osteopontin in a Renal Stone Found in a Hyperuricemic Patient Using 2D-PAGE and LC-MS Analysis | K. Kaneko; T. Yamanobe; K. Nakagomi; K. Mawatari; M. Onoda; S. Fujimori |
| 1131-1134 | EPR Spin Trapping of a Radical Intermediate in the Urate Oxidase Reaction | E. Busi; L. Terzuoli; R. Basosi; B. Porcelli; E. Marinello |
| 1135-1139 | An Unusual Pyridine Nucleotide Accumulating in Erythrocytes: Its Identity, and Positive Correlation with Degree of Renal Failure | E. A. Carrey; R. T. Smolenski; S. M. Edbury; A. Laurence; A. M. Marinaki; J. A. Duley; L. M. Zhu; D. J. A. Goldsmith; H. A. Simmonds |
| 1141-1145 | Identification of Two Novel Mutations in Adenine Phosphoribosyltransferase Gene in Patients with 2,8-Dihydroxyadenine Urolithiasis | Atsuo Taniguchi; Sanae Tsuchida; Shin-Ichi Kuno; Masayuki Mita; Tastuya Machida; Naomasa Ioritani; Chihiro Terai; Hisashi Yamanaka; Naoyuki Kamatani |
| 1147-1152 | Medical Diagnosis, Management and Treatment of Lesch Nyhan Disease | Gillian McCarthy |
| 1153-1160 | The Spectrum of Mutations Causing HPRT Deficiency: An Update | H. A. Jinnah; J. C. Harris; W. L. Nyhan; J. P. O'Neill |
| 1161-1164 | The Motor Disorder of Classic Lesch-Nyhan Disease | Jasper E. Visser; James C. Harris; Gabor Barabas; Gary E. Eddey; H. A. Jinnah |
| 1165-1168 | Clinical and Biochemical Manifestations and Molecular Characterization of the Mutation HPRT Jerusalem | E. Zoref-Shani; Y. Bromberg; J. Hirsch; S. Feinstein; Y. Frishberg; O. Sperling |
| 1169-1172 | Mutations in the Hypoxanthine Guanine Phosphoribosyltransferase Gene (HPRT1) in Asian HPRT Deficient Families | Y. Yamada; K. Yamada; S. Sonta; N. Wakamatsu; N. Ogasawara |
| xi-xiii | List of Contributors | |
| 1-5 | Synthesis and Antiviral Evaluation of Some 3′-Fluoro Bicyclic Nucleoside Analogues | Christopher McGuigan; Antonella Carangio; Robert Snoeck; Graciela Andrei; Erik De Clercq; Jan Balzarini |
| 7-29 | Synthesis and Antiviral Activity of Novel Fluorinated 2′,3′-Dideoxynucleosides | Piyush Kumar; Kazue Ohkura; Jan Balzarini; Erik De Clercq; Koh-ichi Seki; Leonard I. Wiebe |
| 31-39 | An Improved Total Synthesis of Triciribine: A Tricyclic Nucleoside with Antineoplastic and Antiviral Properties | Anthony R. Porcari; Leroy B. Townsend |
| 41-50 | Tandem Mass Spectrometry for Structure Assignments of Wye Nucleosides from Transfer RNA | Shaolian Zhou; Devarasetty Sitaramaiah; Steven C. Pomerantz; Pamela F. Crain; James A. McCloskey |
| 51-66 | Nucleosides. LXV. Synthesis of New Pteridine–N8–Nucleosides | Stefan Matysiak; Bernhard Waldscheck; Wolfgang Pfleiderer |
| 67-76 | 1-Deaza-5′-noraisteromycin | Xueqiang Yin; Stewart W. Schneller |
| 77-88 | How a Modification (8-Aza-3-deaza-2′-deoxyguanosine) Influences the Quadruplex Structure of Hotoda's 6-Mer TGGGAG with 5′- and 3′-End Modifications | Suzana Jakša; Bogdan Kralj; Christophe Pannecouque; Jan Balzarini; Erik De Clercq; Jože Kobe |
| 89-115 | Second Generation of cycloSal-Pronucleotides with Esterase-Cleavable Sites: The ”Lock-In”-Concept | Chris Meier; Manuel F.H. Ruppel; Dalibor Vukadinović; Jan Balzarini |
| 117-126 | Rearrangement Reactions of 1,N2-Isopropenoguanine Cyclonucleosides | Tomasz Zandecki; Jerzy Boryski |
| 127-136 | An Efficient Route to Novel 4,5-Di- and 2,4,5-Tri Substituted Imidazoles from Imidazo[1,5-a]-1,3,5-triazine (5,8-Diaza-7,9-dideazapurine) Derivatives | Bozenna Golankiewicz; Piotr Januszczyk; Joanna Zeidler; Mariusz Popenda |
| 137-147 | Functionalization of Guanosine and 2′-Deoxyguanosine at C6: A Modified Appel Process and SNAr Displacement of Imidazole | Zlatko Janeba; Xiaoyu Lin; Morris J. Robins |
| 149-160 | Biologically Active Antisense Phosphorothioate Oligodeoxyribonucleotides: Synthesis, Characterization, and Studies of 3′-Terminal Phosphorothioate Monoester Analogues | Vasulinga T. Ravikumar; Walt F. Lima; Kent Van Sooy; Brett Turney |
| 161-170 | Synthesis and Biological Activity of 5-Fluorotubercidin | Xiaojing Wang; Punit P. Seth; Ray Ranken; Eric E. Swayze; Michael T. Migawa |
| 171-181 | Improved and Reliable Synthesis of 3′-Azido-2′,3′-dideoxyguanosine Derivatives | Victor A. Timoshchuk; Richard I. Hogrefe; Morteza M. Vaghefi |
| 183-193 | A New Approach for the Synthesis of Novel 5-Substituted Isodeoxyuridine Analogs | Sven Guenther; Vasu Nair |
| 195-205 | Synthesis of Uridine 5′-[2-S-Pyridyl-3-thio-α-d-galactopyranosyl Diphosphate]: Precursors of UDP-Thiogal Sugar Nucleotide Donor Substrate for β-1,4-Galactosyltransferase | Jordan Elhalabi; Kevin G. Rice |
| 207-225 | Intercalating Nucleic Acids: The Influence of Linker Length and Intercalator Type on Their Duplex Stabilities | Ulf B. Christensen; Michael Wamberg; Farag A. G. El-Essawy; Abd El-Hamid Ismail; Christina B. Nielsen; Vyacheslav V. Filichev; Carsten H. Jessen; Michael Petersen; Erik B. Pedersen |
| 227-237 | Regioselective Synthesis of Indazole N1- and N2-(β-d-Ribonucleosides) | Frank Seela; Xiaohua Peng |
| 239-253 | Synthesis of Tunicaminyluracil Derivatives | Satoshi Ichikawa; Akira Matsuda |
| 255-262 | New Sequential-Assignment Routes of Nucleic Acid NMR Signals Using a [5′-13C]-Labeled DNA Dodecamer | Etsuko Kawashima; Takeshi Sekine; Kaoru Umabe; Kazuo Kamaike; Toshimi Mizukoshi; Nobuhisa Shimba; Ei-ichiro Suzuki; Chojiro Kojima |
| 263-271 | Inhibitors of Adenosine Deaminase: Continued Studies of Structure-Activity Relationships in Analogues of Coformycin | Ayub Reayi; Ramachandra S. Hosmane |
| 273-280 | Use of Both Direct and Indirect 13C Tags for Probing Nitrogen Interactions in Hairpin Ribozyme Models by 15N NMR | Anthony J. Shallop; Barbara L. Gaffney; Roger A. Jones |
| 281-289 | The Interaction of Per-O-Acetylated Acyclic 1-(1-Butylindol-3-yl)-1-deoxy-ketoses with Silylated Uracil | S. N. Lavrenov; N. P. Solovyeva; M. I. Reznikova; O. S. Anisimova; M. N. Preobrazhenskaya |
| 291-306 | Tissue Disposition of 5-o-Carboranyluracil—A Novel Agent for the Boron Neutron Capture Therapy of Prostate Cancer | Raymond F. Schinazi; Selwyn J. Hurwitz; Irina Liberman; Yuliya Glazkova; Nicolas S. Mourier; Jeffrey Olson; Thomas Keane |
| 307-316 | Synthesis of 4-Formyl-4-imidazolin-2-one Nucleosides, Isomers of Uridine and 2′-Deoxyuridine | Xiang-Jun Jiang; Thomas I. Kalman |
| 317-337 | Synthesis of Azole Nucleoside 5′-Monophosphate Mimics (P1Ms) and Their Inhibitory Properties of IMP Dehydrogenases | Guangyi Wang; Kandasamy Sakthivel; Vasanthakumar Rajappan; Thomas W. Bruice; Kathleen Tucker; Patrick Fagan; Jennifer L. Brooks; Tiffany Hurd; Janet M. Leeds; P. Dan Cook |
| 339-346 | Effect of Imino Group of a Linker Arm at the C5 Position of a Pyrimidine Nucleoside on the Thermal Stabilities of DNA/DNA and DNA/RNA Duplexes | Hiroaki Ozaki; Masayuki Mine; Kazuo Shinozuka; Hiroaki Sawai |
| 347-359 | Nucleosides. IX. Synthesis of Purine N3,5′-Cyclonucleosides and N3,5′-Cyclo-2′,3′-seconucleosides via Mitsunobu Reaction as TIBO-like Derivatives | Grace Shiahuy Chen; Chien-Shu Chen; Tun-Cheng Chien; Jun-Yen Yeh; Chia-Chi Kuo; Rahul Subhash Talekar; Ji-Wang Chern |
| xv-xxiii | Introduction | |
| 361-373 | Uridine Recognition Motifs of Human Equilibrative Nucleoside Transporters 1 and 2 Produced in Saccharomyces cerevisiae | Mark F. Vickers; Jing Zhang; Frank Visser; Tracey Tackaberry; Morris J. Robins; Lars P. C. Nielsen; Ireneusz Nowak; Stephen A. Baldwin; James D. Young; Carol E. Cass |
| 375-383 | Anti-cowpox Virus Activities of Certain Adenosine Analogs, Arabinofuranosyl Nucleosides, and 2′-Fluoro-arabinofuranosyl Nucleosides | Donald F. Smee; Robert W. Sidwell |
| 385-399 | Synthesis and Evaluation of a Novel Synthetic Phosphocholine Lipid-AZT Conjugate That Double-Targets Wild-Type and Drug Resistant Variants of HIV | Louis S. Kucera; Susan L. Morris-Natschke; Khalid S. Ishaq; Jan Hes; Nathan Iyer; Phillip A. Furman; Ronald A. Fleming |
| 401-410 | Enhanced DNA-Directed Effects of FdUMP[10] Compared to 5FU | William H. Gmeiner; Eric Trump; Cui Wei |
| 411-438 | Synthesis of 2′-Substituted MMI Linked Nucleosidic Dimers: An Optimization Study in Search of High Affinity Oligonucleotides for Use in Antisense Constructs | Didier Peoc'h; Eric E. Swayze; Balkrishen Bhat; Yogesh S. Sanghvi |
| 439-455 | Synthesis of D-Altritol Nucleosides with a 3′-O-Tert-Butyldimethylsilyl Protecting Group | Michael Abramov; Arnaud Marchand; Agnes Calleja-Marchand; Piet Herdewijn |
| 457-470 | Nucleoside Analogues Exerting Antiviral Activity Through a Non-nucleoside Mechanism | Erik De Clercq |
| 471-481 | A2B Adenosine Receptor Agonists: Synthesis and Biological Evaluation of 2-Phenylhydroxypropynyl Adenosine and NECA Derivatives | S. Vittori; S. Costanzi; C. Lambertucci; F. R. Portino; S. Taffi; R. Volpini; K.-N. Klotz; G. Cristalli |
| 483-493 | Monitoring the Intracellular Metabolism of Nucleoside Phosphoramidate Pronucleotides by 31P NMR | Jisook Kim; Daniel P. Drontle; Carston R. Wagner |
| 495-499 | Synthesis of Nucleoside Libraries on Solid Support. I. N2,N6-Disubstituted Diaminopurine Nucleosides | Esmir Gunic; Roberto Amador; Frank Rong; Jeffrey W. Abt; Haoyun An; Zhi Hong; Jean-Luc Girardet |
| 501-507 | Synthesis of Nucleoside Libraries on Solid Support. II. 2,6,8-Trisubstituted Purine Nucleosides Using 8-Bromoguanosine as Precursor | Yung-hyo Koh; Michael B. Landesman; Roberto Amador; Frank Rong; Haoyun An; Zhi Hong; Jean-Luc Girardet |
| 509-520 | Oligonucleotide Conjugates of Nile Red | Igor A. Prokhorenko; Natalia N. Dioubankova; Vladimir A. Korshun |
| 521-530 | Conformational Flexibility in a Triazole Nucleoside Derivative: 4-Cyano-5-cyanomethyl-1-(2,3,5-tri-O-acetyl-β-d-ribofuranosyl)-1,2,3-triazole | Ivan Leban; Marjan Ješelnik; Joachim Sieler; Jože Kobe |
| 489-505 | Oligonucleotides and Derivatives as Gene-Specific Control Agents | Jian-Sheng Sun; Claude Hélène |
| 507-517 | An Industrial Process for Synthesizing Lodenosine (FddA) | Kunisuke Izawa; Satoshi Takamatsu; Satoshi Katayama; Naoko Hirose; Shigetaka Kozai; Tokumi Maruyama |
| 519-534 | Ribonucleotide Reductases: Radical Chemistry and Inhibition at the Active Site | Morris J. Robins |
| 535-546 | Inhibition of Transcription by bisPNA-Peptide Conjugates | Xin Zhao; Kunihiro Kaihatsu; David R. Corey |
| 547-557 | Recent Advances in the Synthesis of Conformationally Locked Nucleosides and Their Success in Probing the Critical Question of Conformational Preferences by Their Biological Targets | Yongseok Choi; Hyung R. Moon; Yuichi Yoshimura; Victor E. Marquez |
| 559-571 | Structures of Non-canonical Tandem Base Pairs in RNA Helices: Review | Hans A. Heus; Cornelis W. Hilbers |
| 573-576 | Pyrazolo[3,4-d]pyrimidine Nucleic Acids: Adjustment of the dA-dT to the dG-dC Base Pair Stability | J. He; G. Becher; S. Budow; F. Seela |
| 577-581 | Oligonucleotide N3′ → P5′ Thio-phosphoramidate Telomerase Template Antagonists as Potential Anticancer Agents | Sergei Gryaznov; Akira Asai; Yuko Oshima; Yoshihiro Yamamoto; Krisztina Pongracz; Ronald Pruzan; Ellen Wunder; Mieczyslaw Piatyszek; Shihong Li; Allison Chin; Calvin Harley; Shiro Akinaga; Yoshinori Yamashita |
| 583-587 | MDPSCL2: A New Protecting Group for Chemoselective Synthesis of 2′-O-Alkylated Guanosines | Suetying Chow; Ke Wen; Yogesh S. Sanghvi; Emmanuel A. Theodorakis |
| 589-592 | Synthesis and Biological Evaluation of Halo-neplanocin A as Novel Mechanism-Based Inhibitors of S-Adenosylhomocysteine Hydrolase | Lak Shin Jeong; Hyung Ryong Moon; Jae Gyu Park; Dae Hong Shin; Won Jun Choi; Kang Man Lee; Hea Ok Kim; Moon Woo Chun; Hee-Doo Kim; Joong Hyup Kim |
| 593-599 | Phosphono Peptide Nucleic Acids with a Constrained Hydroxyproline-Based Backbone | Vladimir A. Efimov; Valeryi N. Klykov; Oksana G. Chakhmakhcheva |
| 601-604 | LNA and α-L-LNA: Towards Therapeutic Applications | Jesper Wengel; Birte Vester; Lars Bo Lundberg; Stephen Douthwaite; Mads D. Sørensen; B. Ravindra Babu; Michael J. Gait; Andrey Arzumanov; Michael Petersen; Jakob T. Nielsen |
| 605-609 | Synthesis and Biological Evaluation of β-D-Pentofuranonucleoside Derivatives of 2-Azidoadenine and 6-Azidopurines | Christophe Mathé; Thierry Lioux; Gilles Gosselin |
| 611-615 | 2′-Fluoro-4′-thio-2′,3′-unsaturated Nucleosides: Anti-HIV Activity, Resistance Profile, and Molecular Modeling Studies | Youhoon Chong; Hyunah Choo; Raymond F. Schinazi; Chung K. Chu |
| 617-621 | Developing Synthetic Methods for Bioactive Phosphorus Compounds Using H-Phosphonate Chemistry: A Progress Report | Martin Bollmark; Tommy Johansson; Martin Kullberg; Johan Nilsson; Jacek Stawinski; Jacek Cieslak; Jadwiga Jankowska; Michal Sobkowski; Marzena Szymczak; Malgorzata Wenska; Adam Kraszewski |
| 623-627 | Preparation and Properties of a New Type of Acyclic, Achiral Nucleoside Analogue | Thomas Boesen; Daniel Sejer Pedersen; Jacob Jensen; Michael T. Munck; Brian M. Nielsen; Asger B. Petersen; Ulla Henriksen; Britta M. Dahl; Otto Dahl |
| 629-633 | A Short, Novel, and Cheaper Procedure for Oligonucleotide Synthesis Using Automated Solid Phase Synthesizer | Quanlai Song; Zhiwei Wang; Yogesh S. Sanghvi |
| 635-639 | Convenient Synthesis of Oligodeoxynucleotides Containing 2′-Deoxy-6-thioinosine | Christine Beuck; Elmar Weinhold |
| 641-644 | A Role for Oligonucleotide-Based RNA-Knock Down Technologies in Functional Genomics | Gabriele Dorn; Jonathan Hall; Dieter Hüsken; Jörg Lange; Pierre Martin; Francois Natt; William L. Wishart; Jan Weiler |
| 645-648 | Properties of Triple Helices Formed by Oligonucleotides Containing 8-Aminopurines | A. Aviñó; M. Frieden; J. C. Morales; B. G. de la Torre; R. Güimil-García; M. Orozco; C. González; R. Eritja |
| 649-652 | Labeling During Cleavage of Nucleic Acids for Their Detection on DNA Chips | A. Laayoun; I. Sothier; L. Menou; E. Bernal-Méndez; M. Kotera; C. Bourget; E. Trévisiol; J. Lhomme; A. Troesch |
| 653-658 | Structural Basis for Topoisomerase I Inhibition by Nucleoside Analogs | William H. Gmeiner; Shuyuan Yu; Richard T. Pon; Philippe Pourquier; Yves Pommier |
| 659-661 | Synthesis of (Z)-(1-Fluoro-2-hydroxymethyl-cyclopropylmethyl)purines | Ju-Hyun Park; Young Rang Lee; Moon Woo Chun; Lak Shin Jeong; Chong-Kyo Lee; Hee-Doo Kim |
| 663-666 | Cyclic Uridine Diphosphate Glucose: A New Pyrimidine Analog of Cyclic ADP Ribose | Marco Cipolletta; Marcella de Champdoré; Lorenzo De Napoli; Giovanni Di Fabio; Anna Messere; Daniela Montesarchio; Gennaro Piccialli |
| 667-669 | A New Approach for Syntheses of 2′,3′-Dideoxy- 2′,3′-dehydronucleosides Using 2,2-Difluoro- 1,3-dimethylimidazolidine (DFI) as a Dehydrating Reagent | Hideki Umetani; Hiroshi Sonoda; Hironori Komatsu |
| 671-673 | Synthesis of New Pseudonucleosides Containing Chiral Cyclosulfamides as Agycone | Malika Berredjem; Nour-Eddine Aouf |
| 675-677 | Synthesis of Thymine Derivatives of 4-Hydroxyvaline | Achamma Abraham; Nicola M. Howarth |
| 679-681 | Doped Natural Phosphate: A New and Environmentally Friendly Catalyst in Nucleoside Synthesis | A. Rochdi; M. Taourirte; N. Redwane; S. Sebti; J. W. Engels; H. B. Lazrek |
| 683-685 | Synthesis of Carbocyclic Analogues of Thymidine | O. R. Ludek; C. Meier |
| 687-689 | The Regiospecific One-Pot Phosphorylation of Either the 5′- or 2′-Hydroxyl in 3′-Deoxycytidines Without Protection: Critical Role of the Base | Peter D. Howes; Martin J. Slater; Katrina Wareing |
| 691-694 | Synthesis of Novel mRNA 5′ Cap-Analogues: Dinucleoside P1, P3-Tri-, P1, P4-Tetra-, and P1, P5-Pentaphosphates | Jacek Jemielity; Janusz Stepinski; Magdalena Jaremko; Dorota Haber; Ryszard Stolarski; Robert E. Rhoads; Edward Darzynkiewicz |
| 695-697 | New Solid Supports Linking Nucleoside Scaffolds | Marcella de Champdoré; Lorenzo De Napoli; Giovanni Di Fabio; Anna Messere; Daniela Montesarchio; Gennaro Piccialli |
| 699-701 | One-Pot Synthesis of an AZT Boranophosphate Conjugated with Tyrosine: A Potential Prodrug Candidate | Ping Li; Barbara Ramsay Shaw |
| 703-705 | Development of a Nucleoside Analog UV Light Sensor | Shiyue Fang; Yousheng Guan; Ernest R. Blatchley III; Lian-Shin Lin; Cheng Yue Shen; Donald E. Bergstrom |
| 707-709 | 4′-C-Methyl-β-D-ribofuranosyl Purine and Pyrimidine Nucleosides Revisited | J. -F. Griffon; D. Dukhan; C. Pierra; S. Benzaria; A. G. Loi; P. La Colla; J. -P. Sommadossi; G. Gosselin |
| 711-713 | A Facile Synthetic Method for 3′-α-Fluoro- 2′,3′-dideoxyadenosine | Satoshi Takamatsu; Satoshi Katayama; Masaki Naito; Keizo Yamashita; Takashi Ineyama; Kunisuke Izawa |
| 715-717 | A Zero-Length Diazirine Photoactive Nucleoside | M. Taranenko; M. Mtchedlidze; N. Sumbatyan; G. Korshunova |
| 719-721 | Synthesis and Biological Evaluation of Pyrimidine Nucleosides Fused with 3′,4′-Tetrahydrofuran Ring | Moon Woo Chun; Myong Jung Kim; Hea Ok Kim; Hyung Ryong Moon; Hee-Doo Kim; Joong Hyup Kim; Lak Shin Jeong |
| 723-725 | Bi- and Tricyclic Nucleoside Derivatives Restricted in S-Type Conformations and Obtained by RCM-Reactions | Nanna Albæk; Jacob Ravn; Morten Freitag; Helena Thomasen; Nanna K. Christensen; Michael Petersen; Poul Nielsen |
| 727-729 | Synthetic Studies on Guanofosfocin: Glycosylation of 8-Oxo-purine Nucleosides via Mitsunobu Reaction | Hideyuki Sugimura; Akiyoshi Koizumi; Wataru Kiyohara |
| 731-733 | A New Type of Acyclic, Achiral Nucleoside Analogue. How Does It Simulate Nucleosides? | Asger B. Petersen; Thomas Boesen; Otto Dahl |
| 735-737 | Rearrangement Reactions of Guanosine Cyclonucleosides and Their Analogs | Jerzy Boryski; Tomasz Zandecki |
| 739-742 | Diastereo- and Enantioselective Synthesis of 1′-C-Branched N, O-Nucleosides | M. G. Saita; U. Chiacchio; D. Iannazzo; A. Corsaro; P. Merino; A. Piperno; T. Previtera; A. Rescifina; G. Romeo; R. Romeo |
| 743-745 | Reactivity Models of 1-N-Vinyluracil and Synthesis of a New Class of Potential Antiviral Agents by the Use of 1,3-Dipolar Cycloaddition Reactions | E. Colacino; G. De Luca; A. Liguori; A. Napoli; C. Siciliano; G. Sindona |
| 747-749 | Selective Metalation of 6-Methylpurines: Synthesis of 6-Fluoromethylpurines and Related Nucleosides | Abdalla E. A. Hassan; William B. Parker; Paula W. Allan; John A. Montgomery; John A. Secrist III |
| 751-753 | Chemo-enzymatic Synthesis of 3-Deoxy-β-D-ribofuranosyl Purines and Study of Their Biological Properties | Vladimir N. Barai; Anatoli I. Zinchenko; Ludmilla A. Eroshevskaya; Elena V. Zhernosek; Jan Balzarini; Erik De Clercq; Igor A. Mikhailopulo |
| 755-758 | Efficient Synthesis of 8-Thiosubstituted Guanine Derivatives as Potential Tools for Biochemical and Biological Studies | Martins Ikaunieks; Marina Madre |
| 759-761 | Synthesis of Carbocyclic Analogues of MECA and NECA 1,2-Disubstituted as Potential Adenosine Receptor Agonists | P. Besada; M. J. González-Moa; C. Terán; M. Teijeira; L. Santana |
| 763-765 | 4-Thiofuranoid Glycals: Versatile Synthons for Stereoselective Synthesis of 4′-Thionucleosides | Kazuhiro Haraguchi; Haruhiko Takahashi; Hiromichi Tanaka |
| 767-769 | Stannylation Approach to the Synthesis of 2′- and 3′-Substituted Analogues of 2′,3′-Didehydro-2′,3′-dideoxynucleosides | Hiroki Kumamoto; Sayoko Onuma; Hiromichi Tanaka |
| 771-773 | Practical Synthesis of D-Cyclopent-2-enone, the Key Intermediate of Carbocyclic Nucleosides | Y. H. Jin; C. K. Chu |
| 775-777 | Covalent Analogues of Nucleobase-Pairs | Michal Hocek; Dalimil Dvořák; Martina Havelková |
| 779-781 | Introduction of a Benzyl Group onto the 2′-OH of 6-Chloropurine 3′-O-Benzoylriboside | Shigetada Kozai; Tomoyo Fuzikawa; Keisuke Harumoto; Tokumi Maruyama |
| 783-785 | Stereocontrolled Synthesis of Diene and Enyne Sugar-Modified Nucleosides and Their Interaction with S-Adenosyl-L-homocysteine Hydrolase | Stanislaw F. Wnuk; Pablo R. Sacasa; Leigh N. Crain; Elzbieta Lewandowska; Jinsong Zhang; Ronald T. Borchardt |
| 787-789 | Purine Derivatives of 1,2-Disubstituted Cyclohexane Analogues of Nucleosides | C. Terán; L. Santana; E. Uriarte; D. Viña; E. De Clercq |
| 791-795 | Study of Different Substituted Cyclic and Acyclic Benzylpronucleotides of d4T Relative to Their Hydrolytic Stability and Antiviral Activity | U. Muus; E. De Clercq; J. Balzarini; L. Naesens; C. Meier |
| 797-799 | Stereochemical Analysis of Diastereomeric 1,3-bis(Adenosine-5′-O-phosphorothioyl)glycerols | Alina Owczarek; Renata Kaczmarek; Barbara Mikołajczyk; Ewa Wasilewska; Dariusz Korczyński; Janina Baraniak; Maria Koziołkiewicz; Wojciech J. Stec; Charles Brenner |
| 801-804 | Design of Mycobacterium tuberculosis Thymidine Monophosphate Kinase Inhibitors | H. Munier-Lehmann; S. Pochet; L. Dugue; O. Dutruel; G. Labesse; D. Douget |
| 805-807 | 5′-O-Ester Prodrugs of Potent and Selective Anti-HIV Agent—2′,3′-Dideoxy-3′-fluoro-2-thiothymidine (S2FLT): Synthesis and Anti-HIV Activity | A. Miazga; N. E. Poopeiko; A. Piasek; M. A. Siweckar; T. Kulikowski |
| 809-812 | 2-Phenylhydroxypropynyladenosine Derivatives as High Potent Agonists at A2B Adenosine Receptor Subtype | C. Lambertucci; R. Volpini; S. Costanzi; S. Taffi; S. Vittori; G. Cristalli |
| 813-815 | Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides | Ruifang Wang; Xinchao Chen; John C. Drach; Earl R. Kern; Jiri Zemlicka |
| 817-819 | Synthesis of Unusual Bicyclic Nucleosides Bearing an Unsaturated Side-Chain, as Potential Inhibitors of Varicella-Zoster Virus (VZV) | O. Bidet; C. McGuigan; G. Andrei; R. Snoeck; E. De Clercq; J. Balzarini |
| 821-823 | Novel Nucleotide Analogues as Potential Substrates for TMPK, a Key Enzyme in the Metabolism of AZT | H. C. Müller; C. Meier; J. Balzarini; J. Reinstein |
| 825-827 | d4TMP Delivery from 7-Substituted cycloSal-d4TMPs | C. Meier; J. T. Renze; J. Balzarini; E. De Clercq |
| 829-831 | Synthesis of New Homo and Heterodimers of 2′,3′-Dideoxyinosine (ddi) Using Ester Linkages | L. Ait Mohamed; M. Taourirte; A. Rochdi; H. B. Lazrek; J. J. Vasseur; J. W. Engels; C. Pannecouque; E. De Clercq |
| 833-836 | Synthesis and Antiviral Activity Assay of Novel (E)-3′,5′-Diamino-5-(2-bromovinyl)-2′,3′,5′-trideoxyuridine | Iván Lavandera; Susana Fernández; Miguel Ferrero; Erik De Clercq; Vicente Gotor |
| 837-839 | Optimization of Antiviral Prodrug Properties Using Combinatorial Methods | Yulia V. Berezovskaya; Mikhail V. Chudinov; Alexander M. Yurkevich |
| 841-843 | Non-inhibition of Acetylcholinesterase by cyclosal Nucleotides | C. Ducho; J. Balzarini; C. Meier |
| 845-847 | Synthesis and Biological Evaluation of a Series of New Cyclohexenyl Nucleosides | Ping Gu; Jordi Morral; Jing Wang; Jef Rozenski; Roger Busson; Arthur Van Aerschot; Erik De Clercq; Piet Herdewijn |
| 849-851 | Synthesis and Antiviral Evaluation of Ribavirin Congeners Containing a Hexitol Moiety | A. Van Aerschot; G. Schepers; R. Busson; J. Neyts; E. De Clercq; P. Herdewijn |
| 853-855 | Dinucleoside Monophosphates Containing AZT and 1-Methyladenosine or 7-Methylguanosine | Boris S. Ermolinsky; Ekaterina V. Efimtseva; Cyrill S. Alexeev; Sergey N. Mikhailov; Jan Balzarini; Erik De Clercq |
| 857-859 | 2′-Deoxy-2′-C-trifluoromethyl β-D-Ribonucleoside Analogues: Synthesis and Antiviral Evaluations | Frédéric Jeannot; Gilles Gosselin; Christophe Mathé |
| 861-863 | Synthesis and Antiviral Evaluation of β-D- and β-L-Pentofuranonucleoside Derivatives Bearing 5-Trifluoromethylcytosine as the Base | Arnaud Marchand; Christophe Mathé; Gilles Gosselin |
| 865-868 | Dinucleoside Polyphosphate NAD Analogs as Potential NMN Adenylyltransferase Inhibitors. Synthesis and Biological Evaluation | P. Franchetti; L. Cappellacci; M. Pasqualini; M. Grifantini; T. Lorenzi; N. Raffaelli; G. Magni |
| 869-872 | A New Tiazofurin Pronucleotide: Synthesis and Biological Evaluation of CycloSaligenyl-Tiazofurin Monophosphate | L. Cappellacci; G. Barboni; P. Franchetti; C. Martini; H. N. Jayaram; M. Grifantini |
| 873-875 | Synthesis of Certain Heterodimers Expected as HIV-1 Reverse Transcriptase Inhibitors | D. Ladurée; E. Sugeac; C. Fossey; S. Schmidt; G. Laumond; A. M. Aubertin |
| 877-881 | Deaza- and Deoxyadenosine Derivatives: Synthesis and Inhibition of Animal Viruses as Human Infection Models | Sauro Vittori; Daniela Salvatori; Rosaria Volpini; Silvia Vincenzetti; Alberto Vita; Sara Taffi; Stefano Costanzi; Catia Lambertucci; Gloria Cristalli |
| 883-885 | Thionucleotides as Inhibitors of Ribonucleotide Reductase | B. Roy; S. Chambert; M. Lepoivre; J. -L. Décout |
| 887-889 | Synthesis of 4′-C-Ethynyl and 4′-C-Cyano Purine Nucleosides from Natural Nucleosides and Their Anti-HIV Activity | Satoru Kohgo; Kohei Yamada; Kenji Kitano; Shinji Sakata; Hiroyuki Hayakawa; Daisuke Nameki; Eiichi Kodama; Masao Matsuoka; Hiroaki Mitsuya; Hiroshi Ohrui |
| 891-894 | Synthesis and Antiviral Evaluation of 2′,3′-Dideoxy-2′-fluoro-3′-C-hydroxymethyl-β-D-arabinofuranosyl Pyrimidine Nucleosides | Abdalla E. A. Hassan; Balakrina S. Pai; Stefania Lostia; Lieven Stuyver; Michael J. Otto; Raymond F. Schinazi; Kyoichi A. Watanabe |
| 895-897 | Investigations of Nucleoside H-Phosphonamidate in the Design of Nucleotide Prodrug | D. Egron; J. -L. Imbach; G. Gosselin; A. -M. Aubertin; C. Périgaud |
| 899-901 | Mononucleoside SATE Glucosyl Phosphorothiolates as a New Series of Pronucleotides | A. Jochum; N. Schlienger; G. Gosselin; J. -L. Imbach; A. -M. Aubertin; C. Périgaud |
| 903-905 | SATE (Aryl) Phosphotriester Series. I. Synthesis and Biological Evaluation | S. Peyrottes; G. Gosselin; A. -M. Aubertin; C. Périgaud |
| 907-909 | SATE (Aryl) Phosphotriester Series. II. Stability Studies and Physicochemical Parameters | G. Coussot; I. Lefebvre; D. Dimalta; S. Peyrottes; A. Pompon; G. Gosselin; C. Périgaud |
| 911-914 | Synthesis and Fluorescent Properties of 6-(4-Biphenylyl)-3,9-dihydro-9-oxo-5H-imidazo[1,2-A]purine Analogues of Acyclovir and Ganciclovir | Tomasz Goslinski; Grazyna Wenska; Bozenna Golankiewicz; Jan Balzarini; Erik De Clercq |
| 915-917 | Synthesis of 5-Azacytidine Nucleosides with Rigid Sugar Moiety as Potential Antitumor Agents | Moon Woo Chun; Myong Jung Kim; Hea Ok Kim; Hee-Doo Kim; Joong Hyup Kim; Hyung Ryong Moon; Lak Shin Jeong |
| 919-921 | Synthesis of Halogenated 9-(Dihydroxycyclopent-4′-enyl) Adenines and Their Inhibitory Activities Against S-Adenosylhomocysteine Hydrolase | Lak Shin Jeong; Jae Gyu Park; Won Jun Choi; Hyung Ryong Moon; Kang Man Lee; Hea Ok Kim; Hee-Doo Kim; Moon Woo Chun; Hea-Young Park; Kilhyoun Kim; Yhun Y. Sheen |
| 923-925 | Design and Synthesis of A3 Adenosine Receptor Ligands, 3′-Fluoro Analogues of Cl-IB-MECA | Hea Ok Kim; Moo Hong Lim; Jae Gyu Park; Hyung Ryong Moon; Kenneth A. Jacobson; Hee-Doo Kim; Moon Woo Chun; Lak Shin Jeong |
| 927-930 | Design and Synthesis of A3 Adenosine Receptor Ligands, 2′-Fluoro Analogues of Cl-IB-MECA | Hea Ok Kim; Jae Gyu Park; Hyung Ryong Moon; Prashantha Gunaga; Moo Hong Lim; Moon Woo Chun; Kenneth A. Jacobson; Hee-Doo Kim; Lak Shin Jeong |
| 931-933 | Bicyclic Nucleoside Inhibitors of Varicella-Zoster Virus: 5′-Chloro and 3′-Chloro Derivatives | G. Luoni; C. McGuigan; G. Andrei; R. Snoeck; E. De Clercq; J. Balzarini |
| 935-937 | Bicyclic Nucleoside Inhibitors of Varicella-Zoster Virus: Synthesis and Biological Evaluation of 2′,3′-Dideoxy- 3′-fluoro and 2′-Deoxy-xylo Derivatives | A. Carangio; C. McGuigan; G. Andrei; R. Snoeck; E. De Clercq; J. Balzarini |
| 939-941 | Synthesis of AZA Analogues of TSAO | Albert Nguyen Van Nhien; Cyrille Tomassi; Christophe Len; José Luis Marco-Contelles; Denis Postel |
| 943-945 | Synthesis, Stability, and Biological Evaluation of 1,3-Dihydrobenzo[c]furan Analogue of d4T and Its SATE Pronucleotide | Christophe Len; Abdelmajid Selouane; Denis Postel; Pierre Villa; Anne-Marie Aubertin; David Egron; Gilles Gosselin; Christian Périgaud |
| 947-949 | N-3 Substituted TSAO Derivatives as a Probe to Explore the Dimeric Interface of HIV-1 Reverse Transcriptase | María-Cruz Bonache; Cristina Chamorro; Sonsoles Velázquez; Erik De Clercq; Jan Balzarini; María-José Camarasa; Ana San-Félix |
| 951-953 | Towards New Thymidine Phosphorylase/PD-ECGF Inhibitors Based on the Transition State of the Enzyme Reaction | E. M. Priego; J. Mendieta; F. Gago; J. Balzarini; E. De Clercq; M. J. Camarasa; M. J. Pérez-Pérez |
| 955-957 | Synthesis of [1′-Fluoro-2′,2′-bis-(hydroxymethyl)-cyclopropylmethyl]purines as Antiviral Agents | Ju-Hyun Park; Myung-Hee Choi; Lak Shin Jeong; Moon Woo Chun; Hee-Doo Kim |
| 959-961 | Unusual Lability of 5′-O-tert-Butyldimethylsilyl Group On 4″-Acyl TSAO Derivatives | Sonia de Castro; María-Jesús Pérez-Pérez; Esther Lobatón; Erik De Clercq; Jan Balzarini; María-José Camarasa; Sonsoles Velázquez |
| 963-966 | Phosphorodiamides as Prodrugs for Antiviral Nucleosides | Alexander V. Shipitsyn; Natalya F. Zakirova; Evgeny F. Belanov; Tatyana R. Pronyaeva; Nina V. Fedyuk; Marina K. Kukhanova; Andrey G. Pokrovsky |
| 967-972 | Synthesis and Biological Evaluation of Some Acyclic 4,6-Disubstituted 1H-Pyrazolo[3,4-d]pyrimidine Nucleosides | O. Moukha-chafiq; M. L. Taha; A. Mouma; H. B. Lazrek; J. J. Vasseur; E. De Clercq |
| 973-976 | Thiated Analogues of 2′,3′-Dideoxy-3′-fluorothymidine and Their Phosphorylated and Phosphonylated Derivatives: Synthesis, Interaction with HIV Reverse Transcriptase, and In Vitro Anti-HIV Activity | A. Miazga; K. Felczak; M. Bretner; M. A. Siwecka; A. Piasek; T. Kulikowski |
| 977-979 | Synthesis and Antimalarial Activity of Novel N6-Substituted Adenosine Derivatives | P. H. Heidler; C. Herforth; A. Link |
| 981-985 | New Lipophilic Derivatives of AZT and d4T 5′-Phosphonates | Elena A. Shirokova; Maxim V. Jasko; Anastasiya L. Khandazhinskaya; Dmitry V. Yanvarev; Yury S. Skoblov; Tatyana R. Pronayeva; Nina V. Fedyuk; Andrey G. Pokrovsky; Marina K. Kukhanova |
| 987-989 | Urinary Modified Nucleosides as Tumor Markers | E. Dudley; F. Lemiere; W. Van Dongen; E. Esmans; A. M. M. El-Sharkawi; D. E. Games; A. G. Brenton; R. P. Newton |
| 991-994 | In Vitro Study of Resistance-Associated Genotypic Mutations to Nucleoside Analogs | N. Gashnikova; O. Plyasunova; Y. Kiseleva; N. Fedyuk; A. Pokrovsky |
| 995-997 | Metabolic and Pharmacological Characteristics of the Bicyclic Nucleoside Analogues (BCNAs) as Highly Selective Inhibitors of Varicella-Zoster Virus (VZV) | R. Sienaert; L. Naesens; A. Brancale; A. Carangio; G. Andrei; R. Snoeck; A. Van Kuilenburg; E. De Clercq; C. McGuigan; J. Balzarini |
| 999-1001 | Characterization of the Catalytic Subunit of the Human Herpesvirus 6 (HHV-6) DNA Polymerase Expressed in an In Vitro Transcription/Translation Assay | L. De Bolle; J. Balzarini; E. De Clercq; L. Naesens |
| 1003-1006 | Monoval-LdC: Efficient Prodrug of 2′-Deoxy-β-L-cytidine (L-dC), A Potent and Selective Anti-HBV Agent | S. Benzaria; C. Pierra; D. Bardiot; E. Cretton-Scott; E. G. Bridges; X. -J. Zhou; D. Standring; G. Gosselin |
| 1007-1009 | Synthesis of 2′-O-Substituted Ribonucleosides | V. Serebryany; L. Beigelman |
| 1011-1015 | Novel Base-Labile Protecting Groups for 5′-Hydroxy Function in Solid-Phase Oligonucleotide Synthesis | Kazuo Kamaike; Takashi Namiki; Etsuko Kawashima |
| 1017-1022 | Progress Towards a Submonomer Synthesis of Peptide Nucleic Acid | R. H. E. Hudson; R. D. Viirre |
| 1023-1027 | Towards a Circular bis-Peptide Nucleic Acid | R. H. E. Hudson; J. Tse |
| 1029-1033 | Nucleobase Modified Peptide Nucleic Acid | R. H. E. Hudson; R. D. Viirre; N. McCourt; J. Tse |
| 1035-1038 | A New Class of Spiegelmers Containing 2′-Fluoro-nucleotides | S. Helmling; E. Moyroud; W. Schroeder; I. Roehl; F. Kleinjung; S. Stark; G. Bahrenberg; C. Gillen; S. Klussmann; S. Vonhoff |
| 1039-1040 | Synthesis of an Asymmetrically Substituted AZA Crown Ether as Metal and Amino Acid Binding Site in DNA Conjugates | Stefan Vogel; Katja Rohr; Otto Dahl; Jesper Wengel |
| 1041-1043 | Nuclease Stability of LNA Oligonucleotides and LNA-DNA Chimeras | Miriam Frieden; Henrik F. Hansen; Troels Koch |
| 1045-1048 | Structural Pre-organization of Peptide Nucleic Acids | Vaijayanti A. Kumar |
| 1049-1052 | Oligomerization Aiming at Phosphonate Analogues of Oligoadenylates | Martina Pressová; Radek Liboska; Miloš Buděšínský; Šárka Králíková; Ivana Kavenová; Ivan Rosenberg |
| 1053-1056 | Ribo-, Xylo-, and Arabino-Configured Adenine-Based Nucleoside Phosphonates: Synthesis of Monomers for Solid-Phase Oligonucleotide Assembly | Ondřej Páv; Miloš Buděšínský; Ivan Rosenberg |
| 1057-1060 | Hybridization Properties of 4′-Branched Oligonucleotides | Radek Liboska; Miloš Buděšínský; Ivana Dvořáková-Kavenová; Ondřej Páv; Ivan Rosenberg |
| 1061-1064 | α-Hydroxyphosphonate Oligonucleotides: A Promising DNA Type? | Šárka Králíková; Miloš Buděšínský; Ivan Rosenberg |
| 1065-1067 | Isosteric Phosphonate Pyrrolidine-Based Dinucleoside Monophosphate Analogues | Václav Vaněk; Miloš Buděšínský; Ivana Kavenová; Markéta Rinnová; Ivan Rosenberg |
| 1069-1071 | Oligonucleotides Containing an Acridine Group Covalently Bonded to the Nucleotide Flanking the 3′-3′ Phosphodiester Junction for Alternate Strand Triple Helix Formation | Bruno Catalanotti; Caterina Fattorusso; Luciano Mayol; Giorgia Oliviero; Gennaro Piccialli; Michela Varra |
| 1073-1075 | New Synthesis of 5-Carboxy-2′-deoxyuridine and Its Incorporation into Synthetic Oligonucleotides | V. Guerniou; D. Gasparutto; S. Sauvaigo; A. Favier; J. Cadet |
| 1077-1079 | Synthesis and Hybridization Properties of Oligonucleotide Analogues Containing Ornithine Backbone Modified with Nucleoalanines | N. Sumbatyan; A. Maksimenko; M. Gottikh; C. Malvy; G. Korshunova |
| 1081-1083 | Synthesis of Thymine-Modified Oligonucleotides | O. Gorchs; A. Grandas; J. Farràs |
| 1085-1087 | 4-Guanidino-2-pyrimidinone Nucleobases: Synthesis and Hybridization Properties | J. Robles; A. Grandas; E. Pedroso |
| 1089-1091 | Synthesis and DNA Binding Properties of DNA-PNA Chimeras | G. Barone; L. De Napoli; G. Di Fabio; E. Erra; C. Giancola; A. Messere; D. Montesarchio; L. Petraccone; G. Piccialli |
| 1093-1095 | Deoxyribonolactone Lesion in DNA: Synthesis of Fluorinated Analogues | Caroline Crey; Pascal Dumy; Jean Lhomme; Mitsuharu Kotera |
| 1097-1099 | Triplex Formation Involving 2′-O,4′-C-Methylene Bridged Nucleic Acid (2′,4′-BNA) with 2-Pyridone Base Analogue: Efficient and Selective Recognition of C:G Interruption | Hidetaka Torigoe; Yoshiyuki Hari; Satoshi Obika; Takeshi Imanishi |
| 1101-1104 | Pyrrolidine PNA-DNA Chimeric Oligonucleotides with Extended Backbone | Vaijayanti A. Kumar; Meena |
| 1105-1108 | Piperidinyl Peptide Nucleic Acids: Synthesis and DNA-Complementation Studies | Pallavi Lonkar; Vaijayanti A. Kumar |
| 1109-1111 | Synthesis and Conformational Properties of O-β-D-Ribofuranosyl-(1″-2′)-guanosine and (Adenosine)-5″-phosphate | Ekaterina V. Efimtseva; Alexandra A. Shelkunova; Sergey N. Mikhailov; Koen Nauwelaerts; Jef Rozenski; Eveline Lescrinier; Piet Herdewijn |
| 1113-1115 | Chemical Incorporation of 1-Methyladenosine, Minor tRNA Component, into Oligonucleotides | E. V. Efimtseva; S. N. Mikhailov; J. Rozenski; R. Busson; A. Van Aerschot; P. Herdewijn |
| 1117-1118 | Oligonucleotides Containing Disaccharide Nucleosides: Synthesis, Physicochemical, and Substrate Properties | S. N. Mikhailov; E. V. Efimtseva; B. S. Ermolinsky; G. V. Bobkov; O. I. Andreeva; A. S. Golubeva; S. N. Kochetkov; A. Van Aerschot; G. Schepers; P. Herdewijn |
| 1119-1121 | Synthesis of Oligonucleotide Building Blocks of 2′-Deoxyguanosine Bearing a C8-Arylamine Modification | S. Gräsl; C. Meier |
| 1123-1125 | α-Hydroxybenzylphosphonate Modified Oligonucleotides: Synthesis, Properties, and a Novel Route via Monomer Building Blocks | Andreas Hohlfeld; Chris Meier |
| 1127-1129 | Determination of the Absolute P-Configuration of a Phthalidyl-Phosphonate Thymidine-Thymidine Dimer | W. Fendrich; C. Meier |
| 1131-1133 | Improved Synthesis of 2′-Amino-LNA | Signe M. Christensen; Christoph Rosenbohm; Mads Sørensen; Lotte-Emilie Larsen; Jesper Wengel; Troels Koch |
| 1135-1137 | Synthesis of an Oligonucleotide Analogue of Ethenoadenosine | Niangoran Koissi; Harri Lönnberg |
| 1139-1141 | Conformationally Restricted Dinucleotides: Tandem Ring-Closing Metathesis and Hydrogenation Approach | Philip Børsting; Poul Nielsen |
| 1143-1145 | α-LNA (α-D-Configured Locked Nucleic Acid) | Nanna K. Christensen; Michael Petersen; Birte Vester; Poul Nielsen |
| 1147-1149 | xylo-Configured Oligonucleotides (XNA, Xylo Nucleic Acids): Synthesis and Hybridization Studies | Nicolai E. Poopeiko; Britta M. Dahl; Jesper Wengel |
| 1151-1153 | RNase H Activation by Stereoregular Boranophosphate Oligonucleotide | Xin Wang; Mikhail Dobrikov; Dmitri Sergueev; Barbara Ramsay Shaw |
| 1155-1157 | Synthesis of a Base-Protected α-L-LNA Guanine Nucleoside | Gilles Gaubert; Jesper Wengel |
| 1159-1161 | Synthesis and Hybridization Properties of Oligodeoxynucleotides Containing 3′-Deoxy-3′-C-methyleneuridine | Dorthe Lindegaard; Jesper Wengel |
| 1163-1165 | Synthesis of a Base-Protected xylo-LNA Adenine Nucleoside | Torsten Bryld; Jesper Wengel |
| 1167-1170 | Synthesis of Modified RNA-Oligonucleotides for Structural Investigations | A. ivković; J. W. Engels |
| 1171-1173 | Synthesis of Dinucleoside Boranophosphates by a Boranophosphotriester Approach | Takeshi Wada; Mamoru Shimizu; Natsuhisa Oka; Kazuhiko Saigo |
| 1175-1178 | Synthesis and Binding Properties of a Homopyrimidine 2′,5′-Linked Xylose Nucleic Acid (2′,5′-XNA) | Kazim A. Agha; Masad J. Damha |
| 1179-1182 | Conjugates of Oligo(2′-O-Methylribonucleotides) with Minor Groove Binders as New Sequence-Specific Agents Recognizing Both Grooves of Double-Stranded DNA | D. Novopashina; A. Sinyakov; V. Ryabinin; A. Venyaminova; A. Boutorine |
| 1183-1185 | Towards a DNA-Like Duplex Without Hydrogen Bonds | Gérald Mathis; Rolf Schütz; Jürg Hunziker |
| 1187-1189 | Pyrrolidino-DNA | Adrian Häberli; Alain Mayer; Christian J. Leumann |
| 1191-1194 | Fluorinated Peptide Nucleic Acid | Marcel Hollenstein; Daniel Gautschi; Christian J. Leumann |
| 1195-1197 | Transition Metal Ligands as Novel DNA-Base Substitutes | Christine Brotschi; Christian J. Leumann |
| 1199-1201 | New Nucleoside Analogues for the Recognition of Pyrimidine-Purine Inversion Sites | Sabrina Buchini; Christian J. Leumann |
| 1203-1206 | Synthetic Studies Towards a Novel, Chemical Stable, Abasic Site Analogue of DNA | Caroline Hirtz; Christian J. Leumann |
| 1207-1210 | Synthesis of a Cyclopentane Amide DNA Analogue and Its Base Pairing Properties | Dae-Ro Ahn; Markus Mosimann; Christian J. Leumann |
| 1211-1213 | Olefinic Peptide Nucleic Acid (OPA) | Daniel Gautschi; Christian J. Leumann |
| 1215-1217 | Synthesis, Biophysical, and Biochemical Properties of PNA-DNA Chimeras | Zoltán Bajor; Gyula Sági; Zsuzsanna Tegyey; László Ötvös |
| 1751-1760 | TT DINUCLEOTIDES CONTAINING AN ISOXAZOLINE MOIETY: SYNTHESIS AND BINDING AFFINITY STUDY | Jong Rock Kong; Sang Kook Kim; Byung Jo Moon; Su Jeong Kim; Byeang Hyean Kim |
| 1761-1774 | CONDENSATION OF TRIFORMYLMETHANE WITH GUANOSINE | Niangoran Koissi; Kari Neuvonen; Tony Munter; Leif Kronberg; Harri Lönnberg |
| 1775-1781 | PREPARATION OF 1-(3-C-(PROPA-1,2-DIENYL)-D-RIBO-PENTOFURANOSYL)URACIL, AN ALLENIC NUCLEOSIDE | Jérôme Dauvergne; Alain Burger; Jean-François Biellmann |
| 1783-1796 | CONFORMATIONAL RIGIDITY INTRODUCED BY 2′,5′-PHOSPHODIESTER LINKS IN DNA | Anil Kumar; Debasis Dass; M. Atreyi; M. V. R. Rao; S. B. Katti |
| 1797-1810 | SYNTHESIS AND BIOLOGICAL ACTIVITY OF 4-SUBSTITUTED 1-[1-(2-HYDROXYETHOXY)- METHYL-1,2,3-TRIAZOL-(4 & 5)-YLMETHYL]-1H-PYRAZOLO[3,4-d]PYRIMIDINES | O. Moukha-Chafiq; M. L. Taha; H. B. Lazrek; C. Pannecouque; M. Witvrouw; E. De Clercq; J. L. Barascut; J. L. Imbach |
| 1811-1821 | SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME 4-SUBSTITUTED 1-[1-(4-HYDROXYBUTYL)-1,2,3-TRIAZOL-(4 & 5)-YLMETHYL]-1H-PYRAZOLO-[3,4-d]PYRIMIDINES | O. Moukha-Chafiq; M. L. Taha; H. B. Lazrek; J. J. Vasseur; C. Pannecouque; M. Witvrouw; E. De Clercq |
| 1823-1830 | SYNTHESIS OF CARBOCYCLIC ANALOGS OF 2′,3′-DIDEOXYSANGIVAMYCIN, 2′,3′-DIDEOXYTOYOCAMYCIN, AND 2′,3′-DIDEOXYTRICIRIBINE | Kristjan S. Gudmundsson; Zhicheng Wang; Susan M. Daluge; Paul L. Feldman |
| 1831-1841 | SYNTHESIS OF 5-METHYLAMINO-2′-DEOXYURIDINE DERIVATIVES | Bruno Catalanotti; Aldo Galeone; Luciano Mayol; Giorgia Oliviero; Daniela Rigano; Michela Varra |
| 1843-1849 | THE SYNTHESIS OF DITHYMIDINE BORANOPHOSPHATE BY THE OXATHIAPHOSPHOLANE APPROACH | Andrzej Okruszek; Agnieszka Sierzchała; Katarzyna Żmudzka; Wojciech J. Stec |
| 1851-1858 | SITE SPECIFIC INCORPORATION OF 6-AZAURIDINE INTO THE GENOMIC HDV RIBOZYME ACTIVE SITE | Adegboyega K. Oyelere; Scott A. Strobel |
| 1859-1870 | 5′-BIS-PYRENYLATED OLIGONUCLEOTIDES DISPLAY ENHANCED EXCIMER FLUORESCENCE UPON HYBRIDIZATION WITH DNA AND RNA | E. Kostenko; M. Dobrikov; N. Komarova; D. Pyshniy; V. Vlassov; M. Zenkova |
| 1871-1879 | EFFICIENT ASSESSMENT OF MODIFIED NUCLEOSIDE STABILITY UNDER CONDITIONS OF AUTOMATED OLIGONUCLEOTIDE SYNTHESIS: CHARACTERIZATION OF THE OXIDATION AND OXIDATIVE DESULFURIZATION OF 2-THIOURIDINE | E. Sochacka |
| 1881-1889 | O-GLYCOSIDES OF N-HYDROXYINDOLES[1] | S. N. Lavrenov; A. M. Korolev; M. N. Preobrazhenskaya |
| 1891-1902 | SYNTHESIS AND ANTIVIRAL EVALUATION OF N-GLYCOSIDES DERIVED FROM 6-AMINO-3-ARYL-2-METHYL-4-(3H)-QUINAZOLINONES | Mohamed A. Saleh; Youssef A. Abbas; Fouad Eabdel-Hai; Shaban A. Youssef |
| 1201-1204 | EXTRA STABLE 2′,5′-LINKED RNA LOOPS | Rami N. Hannoush; Masad J. Damha |
| 1205-1209 | EFFECT OF SUBSTITUTING ARABINONUCLEOSIDES FOR DEOXYNUCLEOTIDES IN THE DNA PRIMING STRAND ON THE POLYMERASE ACTION OF HIV-1 RT | Anne M. Noronha; Dominique Arion; Michael A. Parniak; Masad J. Damha |
| 1211-1217 | MOLECULAR MODELLING OF 2′-OH MEDIATED HYDROGEN BONDING IN RIBONUCLEOS(T)IDES BY NMR CONSTRAINED AM1 AND MMX CALCULATIONS | Parag Acharya; Irina Velikian; Sandipta Acharya; Jyoti Chattopadhyaya |
| 1219-1223 | DO THE 16 MER, 5′-GUGGUCUGAUGAGGCC-3′ AND THE 25 MER, 5′-GGCCGAAACUCGUAAGAGUCACCAC-3′, FORM A HAMMERHEAD RIBOZYME STRUCTURE IN PHYSIOLOGICAL CONDITIONS? AN NMR AND UV THERMODYNAMIC STUDY | Edouard Zamaratski; Anna Trifonova; Parag Acharya; Johan Isaksson; Tatiana Maltseva; Jyoti Chattopadhayaya |
| 1225-1228 | THE NMR CONFORMATION STUDY OF THE COMPLEXES OF DEOXYCYTIDINE KINASE (dCK) AND 2′-DEOXYCYTIDINE/2′-DEOXYADENOSINE | T. Maltseva; E. Usova; S. Eriksson; J. Milecki; A. Földesi; J. Chattopadhayaya |
| 1229-1233 | AN ENERGETIC CORRELATION OF AB INITIO AND NMR STUDIES OF THE 3′-GAUCHE EFFECT IN 3′-SUBSTITUTED THYMIDINES | Parag Acharya; Christophe Thibaudeau; Jyoti Chattopadhyaya |
| 1235-1238 | PROMOTION OF TRIPLEX FORMATION BY 2′-O,4′-C-METHYLENE BRIDGED NUCLEIC ACID (2′,4′-BNA) MODIFICATION: THERMODYNAMIC AND KINETIC STUDIES | Hidetaka Torigoe; Satoshi Obika; Takeshi Imanishi |
| 1239-1241 | A DNA-BINDING PEPTIDE FROM A PHAGE DISPLAY LIBRARY | Julian Wölcke; Elmar Weinhold |
| 1243-1246 | INHIBITION OF HUMAN TELOMERASE BY L-ENANTIOMERS OF NATURAL 2′-DEOXYRIBONUCLEOSIDE 5′-TRIPHOSPHATES | Toyofumi Yamaguchi; Rieko Yamada; Aki Tomikawa; Koichi Shudo; Motoki Saito; Fuyuki Ishikawa; Mineo Saneyoshi |
| 1247-1250 | MECHANISTIC STUDIES TO UNDERSTAND THE INHIBITION OF WILD TYPE AND MUTANT HIV-1 REVERSE TRANSCRIPTASE BY CARBOVIR-TRIPHOSPHATE | Adrian S. Ray; Karen S. Anderson |
| 1251-1254 | ACCELERATION OF NUCLEIC ACID HYBRIDIZATION ON DNA MICROARRAYS DRIVEN BY pH TUNABLE MODIFICATIONS | Peiming Zhang; Natalia Briones; Chang-Gong Liu; Charles K. Brush; Tom Powdrill; Yuri Belosludtsev; Mike Hogan |
| 1255-1258 | LABORATORY DIAGNOSIS OF RESPIRATORY DISEASES: PCR VERSUS SEROLOGY | H. Haaheim; L. Vorland; T. J. Gutteberg |
| 1259-1262 | PHOTOSENSITIZED AND CATALYTIC OXIDATION OF DNA BY METALLOPHTHALOCYANINE-OLIGONUCLEOTIDE CONJUGATES | V. V. Koval; A. A. Chernonosov; T. V. Abramova; T. M. Ivanova; O. S. Fedorova; V. M. Derkacheva; E. A. Lukyanets |
| 1263-1266 | SYNTHESIS OF 2′,3′-DIDEOXY-2′,3′-DIDEHYDRO NUCLEOSIDES VIA A SERENDIPITOUS ROUTE | Z. Guo; Y. S. Sanghvi; L. E. Brammer Jr.; T. Hudlicky |
| 1267-1270 | UNEXPECTED RESULTS AND RECOURSE IN PROCESS OPTIMIZATION OF NUCLEOSIDE 3′-O-SUCCINATES | Quanlai Song; Yogesh S. Sanghvi |
| 1271-1274 | A NEW FACILE METHOD FOR SPIN-LABELING OF OLIGONUCLEOTIDES | Thorsten Strube; Olav Schiemann; Fraser MacMillan; Thomas Prisner; Joachim W. Engels |
| 1275-1278 | PHENYLALKYL BACKBONE MODIFIED OLIGODEOXYNUCLEOTIDES, THEIR SYNTHESIS AND THE INFLUENCE OF THE ALKYL CHAIN LENGTH | Stefan Amberg; Joachim W. Engels |
| 1279-1282 | SYNTHESIS AND BASE PAIRING PROPERTIES OF 9-DEAZAPURINE N7-NUCLEOSIDES IN OLIGONUCLEOTIDE DUPLEXES AND TRIPLEXES | P. Leonard; T. Wiglenda; F. Seela |
| 1283-1286 | PARALLEL DNA CONTAINING PYRAZOLO[3,4-D]PYRIMIDINE ANALOGUES OF ISOGUANINE | F. Seela; R. Kröschel; Y. He |
| 1287-1289 | BRIDGED CYCLIC OLIGORIBONUCLEOTIDES—TOWARDS MODELS FOR CODON-ANTICODON PAIRING | R. Micura; W. Pils; K. Grubmayr; M. -O. Ebert; B. Jaun |
| 1291-1293 | LARGE-SCALE MANUFACTURING OF ALL FOUR 2′-DEOXYNUCLEOSIDES VIA NOVEL STRATEGIES INCLUDING A CHEMO-ENZYMATIC PROCESS | Hironori Komatsu; Hirokazu Awano; Hiroharu Tanikawa; Kiyoshi Itou; Ichirou Ikeda |
| 1295-1298 | KINETIC STUDIES OF THE DEGRADATION OF OXYCARBONYLOXYMETHYL PRODRUG OF ADEFOVIR AND TENOFOVIR IN SOLUTION | Reza Oliyai; Lung-Chi Yuan; Terry Dahl |
| 1299-1302 | DEALKYLATION OF PHOSPHONATE ESTERS WITH CHLOROTRIMETHYLSILANE | A. J. Gutierrez; E. J. Prisbe; J. C. Rohloff |
| a-b | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 19, Number 5-6 | |
| 845-849 | Synthesis and Antiviral Activity of 3-(β-D-Ribofuranosyl)-1,2,4-oxadiazole-5-carboxamide | Ram Pratap; V. N. Yarovenko |
| 851-866 | Synthesis of N,N-Dialkylaniline-2′-deoxyuridine Conjugates for DNA-Mediated Electron Transfer Studies | E. Charles Kerr; E Bruce Eaton; L. Thomas Netzel |
| 867-879 | Synthesis of Unsaturated Carboacyclic Nucleoside Analogues via Mitsunobu Reactions | Jinfa Du; Guangyi Wang |
| 881-889 | Synthesis of [bis(Inosine-5′)]-tetraphosphate and [bis(Inosine-5′)]-pentaphosphate Analogues Bearing the Residues of Methylenediphosphonic Acid | A. V. Shipitsyn; N. B. Tarussova; E. A. Shirokova; A. A. Krayevsky |
| 891-902 | Kinetic Studies on CE(IV)-Induced Hydrolysis of Single-Stranded and Double-Stranded Oligonucleotides | Tomoyuki Igawa; Jun Sumaoka; Makoto Komiyama |
| 903-915 | Synthesis and NMR Characterization of Diastereomeric CPSMeG Derivatives | Daisy Machytka; Gyula Sági; MÁRia Kajtár-peredy; Eszter Gács-baitz |
| 917-933 | The Chemical Synthesis of Oligoribonucleotides with Selectively Placed 2′-O-Phosphates | Ryszard Kierzek; Michelle A. Steiger; Sherry L. Spinelli; Douglas H. Turner; Eric M. Phizicky |
| 935-940 | A Convenient Synthesis of A Novel Nucleoside Analogue: 4-(δ-Diformyl-methyl)-1-(β-D-ribofuranosyl)-2-pyrimidinone | Kui Gao; Leslie E. Orgel |
| 941-954 | Studies on Epimeric D-xylo-and D-lyxo-Tetritol-yl-2-phenyl-2H-1,2,3-triazoles. Synthesis and Anomeric Configuration of 4-(α- and β-D-Threofuranosyl)-2-phenyl-2H-1,2,3-triazole C-Nucleoside Analogs | Mohammed A. E. Sallam; Farida F. Louis; John M. Cassady |
| 955-962 | Investigation of a Facile Synthetic Method for Phosphorothioate Dimer Synthons In Oligonucleotide Phosphorothioates Synthesis | Takanori Miyashita; Kohei Yamada; Kazuhiko Kondo; Kenya Mori; Kazuo Shinozuka |
| 963-975 | Inhibition of Cell Growth and Proliferation in Human Glioma Cells and Normal Human Astrocytes Induced by 8-Cl-cAMP and Tiazofurin | M. Pesic; K. Drabek; C. Esler; S. Ruzdijic; V. Pejanovic; Z. Pietrzkowski |
| 977-994 | The Nonenzymatic Hydrolysis of Oligoribonucleotides VII. Structural Elements Affecting Hydrolysis | Arkadiusz Bibillo; Marek Figlerowicz; Krzysztof Ziomek; Ryszard Kierzek |
| 995-1003 | Prooligonucleotides Exhibit Less Serum-Protein Binding Than Phosphodiester and Phosphorothioate Oligonucleotides | Guilhem Tosquellas; Anton Bryksin; Karine Alvarez; François Morvan; Jean-Jacques Vasseur; Bernard Rayner; Elena Rykova; Pavel Laktionov; Valentin Vlassov; Jean-Louis Imbach |
| 1005-1015 | Synthesis of 6-Alkyl- and Arylamino-9-(tetrahydro-2-pyranyl)purines via 6-Methylsulfonylpurine | José Daniel Figueroa Villar; Marita Almeida Motta |
| 1017-1031 | Synthesis and Antiviral Activity of C-5 Substituted Analogues of D4T Bearing Methylamino- or Methyldiamino-Linker Arms | D. Gavriliu; C. Fossey; G. Fontaine; S. Benzaria; A. Ciurea; Z. Delbederi; B. Lelong; D. Ladurée; A. M. Aubertin; A. Kirn |
| 1033-1054 | Synthesis, Mechanism and Fluorescence Properties of 8-(Aryl)-3-β-D-Ribofuranosylimidazo[2,1-i]purine 5′-Phosphate Derivatives | Bilha Fischer; Eihab Kabha; Fernand-Pierre Gendron; Adrien R. Beaudoin |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 19, Number 3 | |
| 515-531 | Synthesis and Properties of Uniquely Modified Oligoribonucleotides: Yeast TrnaPhe Fragments with 6-Methyluridine and 5,6-Dimethyluridine at Site-Specific Positions | Elzbieta Sochacka; Grazyna Czerwinska; Richard Guenther; Robert Cain; Paul F. Agris; Andrzej Malkiewicz |
| 533-543 | Influence of Diastereomeric Ratios of Deoxyribonucleoside Phosphoramidites on the Synthesis of Phosphorothioate Oligonucleotides | Z. S. Cheruvallath; H. Sasmor; D. L. Cole; V. T. Ravikumar |
| 545-558 | Development of a Purification Procedure for the Isolation of Nucleosides from Urine Prior to Mass Spectrometric Analysis | E. Dudley; S. El-shakawi; D. E. Games; R. P. Newton |
| 559-565 | A Convenient Synthesis of 2′-Deoxy-2-fluoroadenosine; a Potential Prodrug for Suicide Gene Therapy | Abdalla E. A. Hassan; Anita T. Shortnacy-fowler; John A. Montgomery; John A. Secrist III |
| 567-584 | Synthesis and Biological Activities of New Carbaacyclonucleosides and 1′-Oxaacyclonucleosides Related to Clitocine | Corinne Bacchelli; Roger Condom; Nadia Patino; Anne-Marie Aubertin |
| 585-591 | Formation and Reactivity of 2,4-Ditriazolyl Pyrimidine C-Nucleoside Derived from Pseudouridine | Natalia Dyatkina; Alexander Khorlin; Kyoichi A. Watanabe |
| 593-601 | Synthesis of Oligodeoxyribonucleotide Bearing 2′-S-Alkyl Residue and its Effect on the Duplex Stability | Hiroaki Ozaki; Yuichi Sato; Sadaji Azuma; Hiroaki Sawai |
| 603-618 | Synthesis and Biological Evaluation of 1,3-Oxathiolane 5-Azapyrimidine, 6-Azapyrimidine, and Fluorosubstituted 3-Deazapyrimidine Nucleosides | Mao-Chin Liu; Mei-Zhen Luo; Diane E. Mozdziesz; Tai-Shun Lin; Ginger E. Dutschman; Elizabeth A. Gullen; Yung-Chi Cheng; Alan C. Sartorelli |
| 619-628 | Efficient Synthesis of Carbocyclic Nucleoside, (±)-Homocarbovir Via π-Allylpalladium Complex Formation from the Allyl N,N-Ditosylimide Substrate | Hakjune Rhee; Dong-Oh Yoon; Michael E. Jung |
| 629-635 | Stereoselective Synthesis and X-Ray Structure of 1-(4-O-Benzyl-1,5-anhydro-2,3-dideoxy-D-arabino-hex-1-enitol-3-yl)-4-methoxy-1H-pyrimidin-2-one | Hideyuki Sugimura |
| 637-650 | Syntheses, Crystal Structures, and Hydrogen Bonding Patterns of 3′-C-Methylenecarboxylic-3′-deoxythymidine and 3′-C-Methyleneamidilylic-3′-deoxythymidine | Joong Young Kim; Byeang Hyean Kim |
| 651-690 | The Latest Progress in the Synthesis of Carbocyclic Nucleosides | Xue-Feng Zhu |
| 691-702 | Cellular Pharmacology of the D- and L-Enantiomers of β-5-o-Carboranyl-2′-deoxyuridine | Selwyn J. Hurwitz; Li; Alessandra Eleuteri; Janis Wright; Josef Moravek; Raymond F. Schinazi |
| 703 | Erratum | |
| xiii-xiv | Guest Editorial | T. A. Krenitsky; G. W. Koszalka |
| xv-xvii | Biographical Sketch | William H. Prusoff |
| a-b | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 19, Number 1-2 | |
| 1-12 | The “β-Fluorine Effect” in the Non-Metal Hydride Radical Deoxygenation of Fluorine-Containing Nucleoside Xanthates | Maqbool A. Siddiqui; John S. Driscoll; Elie Abushanab; James A. Kelley; Joseph J. Barchi Jr.; Victor E. Marquez |
| 13-29 | Conformation and Local Environment of Nucleotides Bound To Hiv Type 1 Reverse Transcriptase (HIV-1 RT) in The Ground State | George R. Painter; C. Webster Andrews; Phillip A. Furman |
| 31-37 | Synthesis of (Z)- and (E)-9-[(2-Hydroxyethylidene)cyclopropyl]adenine—New Methylenecyclopropane Analogues of Adenosine and Their Substrate Activity for Adenosine Deaminase | Yao-Ling Qiu; Mohamad B. Ksebati; Jiri Zemlicka |
| 39-68 | Synthesis of 4-Substituted Imidazo[4,5-d][1,2,3]triazine (2-Azapurine)nucleosides | Steven Krawczyk; Michael T. Migawa; John C. Drach; Leroy B. Townsend |
| 69-86 | Synthesis of Amide-Linked [(3′)CH2CO-NH(5′)] Nucleoside Analogues of Small Oligonucleotides | Morris J. Robins; Bogdan Doboszewski; Bradley L. Nilsson; Matt A. Peterson |
| 87-100 | Synthesis and Antiviral Activity of Amino Acid Carbamate Derivatives of AZT | Shu-Ling Chang; George Griesgraber; Timothy W. Abraham; Tullika Garg; Heng Song; Cheryl L. Zimmerman; Carston R. Wagner |
| 101-123 | Synthesis and Evaluation of a Series of 2′-Deoxy Analogues of The Antiviral Agent 5,6-Dichloro-2-Isopropylamino-1-(β-L-Ribofuranosyl)-1H-Benzimidazole (1263W94) | Joseph H. Chan; Stanley D. Chamberlain; Karen K. Biron; Michelle G. Davis; Robert J. Harvey; Dean W. Selleseth; Ronna E. Dornsife; Ernest H. Dark; Lloyd W. Frick; Leroy B. Townsend; John C. Drach; George W. Koszalka |
| 125-153 | Design, Synthesis, and Antiviral Evaluation of 2-Deoxy-D-Ribosides of Substituted Benzimidazoles as Potential Agents for Human Cytomegalovirus Infections | Ruiming Zou; Etsuko Kawashima; George A. Freeman; George W. Koszalka; John C. Drach; Leroy B. Townsend |
| 155-174 | Benzimidazole 2′-Isonucleosides: Design, Synthesis, and Antiviral Activity of 2-Substituted-5,6-Dichlorobenzimidazole 2′-Isonucleosides | G. A. Freeman; D. W. Selleseth; J. L. Rideout; R. J. Harvey |
| 175-187 | Nucleosides and Nucleotides. 192. Toward the Total Synthesis of Cyclic ADP-Carbocyclic-Ribose. Formation of the Intramolecular Pyrophosphate Linkage by a Conformation-Restriction Strategy in a Syn-form Using a Halogen Substitution at the 8-Position of the Adenine Ring | Yuji Sumita; Michiyo Shirato; Yoshihito Ueno; Akira Matsuda; Satoshi Shuto |
| 189-203 | Investigation of The Kinetics of Degradation of Hexopyranosylated Cytosine Nucleosides Using Liquid Chromatography | Grace N. Thoithi; Ann Van Schepdael; Roger Busson; Gerard Janssen; Arthur Van Aerschot; Piet Herdewijn; EugÈNe Roets; Jos Hoogmartens |
| 205-217 | Synthesis and Antiviral Evaluation of Unnatural β-L-Enantiomers of 3′-Fluoro- and 3′-Azido-2,3′-dideoxyguanosine Derivatives | Arnaud Marchand; Christophe Mathé; Jean-Louis Imbach; Gilles Gosselin |
| 219-236 | Synthesis of L-3′-Hydroxymethylribonucleosides | John S. Cooperwood; Vincent Boyd; Giuseppe Gumina; Chung K. Chu |
| 237-251 | Pyrrolo[2,3-d]Pyrimidine Nucleosides: Synthesis and Antitumor Activity of 7-Substituted 7-Deaza-2′-Deoxyadenosines | Frank Seela; Matthias Zulauf; Shih-Fong Chen |
| 253-268 | Synthesis and Antiviral Activities of Enantiomeric 1-[2-(Hydroxymethyl) Cyclopropyl] Methyl Nucleosides | Claire Pierra; Sureyya Olgen; Sócrates C. H. Cavalcanti; Yung-Chi Cheng; Raymond F. Schinazi; Chung K. Chu |
| 269-273 | Carbocyclic 5′-Noruridine | Vishnumurthy R. Hegde; Katherine L. Seley; Stewart W. Schneller |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 18, Number 9 | |
| 1911-1928 | Synthesis of Chiral Carbocyclic Ribonucleotides | Vincent D. Antle; Carol A. Caperelli |
| 1929-1933 | Base Modified Oligodeoxynucleotides. II. Increase of Stability to Nucleases by 5-Alkyl-, 5-(1-Alkenyl)-, and 5-(1-Alkynyl)-pyrimidines | L. Ötvös; J. Sági; Gy. Sági; A. Szemz |
| 1935-1944 | Identification of a Good C-MYC Antisense Oligodeoxynucleotide Target Site and the Inactivity at This Site of Novel NCH Triplet-Targeting Ribozymes | Richard V. Giles; David G. Spiller; Richard E. Clark; David M. Tidd |
| 1945-1960 | Application of Oligonucleoside Methylphosphonates in the Studies on Phosphodiester Hydrolysis by Serratia Endonuclease | Tushar Kumar Srivastava; Peter Friedhoff; Alfred Pingoud; S. B. Katti |
| 1961-1976 | Homologues of Isomeric Dideoxynucleosides as Potential Antiviral Agents: Synthesis of Isodideoxy-Nucleosides with a Furanethanol Sugar Moiety | Xiaoping Zheng; Vasu Nair |
| 1977-1984 | Asymmetric Synthesis of 4′-Methyl-2′,3′-dideoxynucleosides | Frederick A. Luzzio; Alexander V. Mayorov; Michael E. Menes; William L. Champion Jr. |
| 1985-1994 | Synthesis and Antiviral Activity of 1,5-and 1,3-Dialkyl-1,2,4-triazole C-Nucleosides Derived from 1-(Chloroalkyl)-1-aza-2-azoniaallene Salts | Yaseen A. Al-soud; Wasfi A. Al-masoudi; Rajab Abu El-halawa; Najim Al-masoudi |
| 1995-2016 | Synthesis of Iodoaminoimidazole Arabinoside (IAIA): A Potential Reductive Metabolite of the Spect Imaging Agent, Iodoazomycin Arabinoside (IAZA) | Herbert C. Lee; Piyush Kumar; Leonard I. Wiebe; Robert McDonald; John R. Mercer; Kazue Ohkura; Koh-Ichi Seki |
| 2017-2030 | Evaluation of Oligonucleotides Containing Two Novel 2′-O-Methyl Modified Nucleotide Monomers: A 3′-C-Allyl and a 2′-O-3′-C-Linked Bicyclic Derivative | Henrik M. Pfundheller; Alexei A. Koshkin; Carl Erik Olsen; Jesper Wengel |
| 2031-2042 | Synthesis and Nuclease Stability of Dinucleotides Containing an Anti- conformationally Constrained Acyclic Thymidine | Ling-Yih Hsu; Kuo-Tsao Yang |
| 2043-2049 | Nucleosides. II. Synthesis and Properties of 3,4-Diaryl-4,5-dihydro-1-(β-D-ribofuranosyl)-1,2,4-triazole-5-thiones | Mosselhi A. N. Mosselhi |
| 2051-2069 | Evaluation of Different Types of End-Capping Modifications on the Stability of Oligonucleotides Toward 3′- and 5′-Exonucleases | Daniela Pandolfi; Francesca Rauzi; Massimo L. Capobianco |
| 2071-2091 | Physico-chemical and Biological Properties of Antisense Phosphodiester Oligonucleotides with Various Secondary Structures | Andrei V. Maksimenko; Marina B. Gottikh; Valerie Helin; Zoe A. Shabarova; Claude Malvy |
| 2093-2108 | Hydrolytic Reactions of 3′-Deoxy-3′-thioinosylyl-(3′→ >5′)-uridine; An RNA Dinucleotide Containing a 3′-S-Phosphorothiolate Linkage | Mohamed I. Elzagheid; Mikko Oivanen; Karel D. Klika; Bryan C. N. M. Jones; Richard Cosstick; Harri Lönnberg |
| 2109-2120 | A Simple and Efficient Procedure for the Synthesis of an Alendronate- Oligonucleotide Conjugate via a Carbamate Linker | M. Lecouvey; C. Dufau; El D. Manouni; Y. Leroux |
| 2121-2126 | Palladium-Catalyzed Animation of 6-Chloropurine. Synthesis of N6-Substituted Adenosine Analogues | Judith Barends; Johannes van der Linden; Floris Van Delft; Gerrit-Jan Koomen |
| 2127-2139 | Regioselective N1-Alkylation of Guanosine Derivatives Protected at N2 by an N,N-Dialkyl Amidine Group | Stéphane P. Vincent; Charles Mioskowski; Luc Lebean |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 18, Number 4-5 | |
| xxxix-xl | Preface | Gilles Gosselin |
| 509-519 | Studies Designed to Increase the Stability and Antiviral Activity (HCMV) of the Active Benzimidazole Nucleoside, TCRB | Leroy B. Townsend; Kristjan S. Gudmundsson; Susan M. Daluge; Jiong J. Chen; Zhijian Zhu; George W. Koszalka; Leslie Boyd; Stanley D. Chamberlain; George A. Freeman; Karen K. Biron; John C. Drach |
| 521-530 | Conformationally Restricted Nucleosides. The Reaction of Adenosine Deaminase with Substrates Built on a Bicyclo[3.1.0]hexane Template | Victor E. Marquez; Pamela Russ; Randolph Alonso; Maqbool A. Siddiqui; Kye-Jung Shin; Clifford George; Marc C. Nicklaus; Fang Dai; Harry Ford Jr. |
| 531-536 | Conformationally Locked Nucleoside Analogs. Synthesis of 2′-Deoxy-2′-C, 4′-C-Bridged Bicyclic Nucleosides | Guangyi Wang; Esmir Gunic |
| 537-540 | New Classes of Fluorinated L-Nucleosides; Synthesis and Antiviral Activity | Kyeong Lee; Yongseok Choi; Joon H. Hong; Raymond F. Schinazi; Chung K. Chu |
| 541-546 | Synthesis and Testing of New Modified Nucleosides | Michael E. Jung; Christopher J. Nichols; Oliver Kretschik; Yue Xu |
| 547-553 | Mechanistic and Synthetic Aspects of the C-1′ Radicals in Modified Nucleosides | Chryssostomos Chatgilialoglu |
| 555-556 | Recent Advances in the Synthesis of 6-Vinyl-N,N-Dialkylcytosine Derivatives | Maurizio Botta; Raffaele Saladino; Luigi Stasi; Umberto Ciambecchini; Rosario Nicoletti |
| 557-558 | A Novel Approach for the Synthesis of seco C-Nucleoside Analogues | Laila F. Awad; El Sayed H. El Ashry |
| 559-563 | Simple and Stereoselective Syntheses of Nucleoside Analogues with a Benzo[c]furan Glycone Moiety | David F. Ewing; Noureddine Fahmi; Grahame Mackenzie; Alessandra Pranzo |
| 565-567 | A Convenient Approach to N-3 Alkylation of 9-Substituted Guanines | Tomasz Ostrowski; Joanna Zeidler; Tomasz Goelizski; Bozenna Golankiewicz |
| 569-570 | A New Series of Mechanism-Based Inhibitors of S-Adenosyl-L-Homocysteine Hydrolase from Beef Liver | Corinne Vandenplas; Danielle Guillerm; Georges Guillerm |
| 571-572 | Synthesis and Antiviral Activity of L-2′-Deoxy-2′-up-fluoro-4′-thionucleosides | Lak Shin Jeong; Hyung Ryong Moon; Su Jeong Yoo; Sun Nan Lee; Hee-Doo Kim; Moon Woo Chun |
| 573-574 | Synthesis and Polymerase Incorporation Properties of a Tricyclic Pyrrolopyrimidine Related to N6-Hydroxy-2′-deoxyadenosine | F. Hill; D. Loakes; C. L. Smith; D. M. Williams; D. M. Brown |
| 575-576 | Synthesis and Biological Evaluation of New Enantiomers of 5-O-Carboranyl Pyrimidine Nucleosides | Nicolas Mourier; Alessandra Eleuteri; Raymond F. Schinazi |
| 577-579 | Synthesis of Novel Isomeric Dideoxydidehydronucleosides | Vasu Nair; Sanjib Bera; Travis Mickle; Serge Van Calenbergh |
| 581-583 | Synthesis of Isoxazolidino Analogues of 2′,3′-Dideoxynucleosides | Evelina Colacino; Antonella Converso; Antonio De Nino; Antonella Leggio; Angelo Liguori; Loredana Maiuolo; Anna Napoli; Antonio Procopio; Carlo Siciliano; Giovanni Sindona |
| 585-586 | Lithiation-Stannylation Chemistry of Nucleosides | Hiromichi Tanaka; Hiroki Kumamoto; Satoru Shindoh; Hiroyuki Hayakawa; Keisuke Kato; Tadashi Miyasaka |
| 587-590 | Coupling of 2,6-Dichloropurine and 2,6-Dichlorodeazapurines with Ribose and Ribose Modified Sugars | S. Vittori; E. Camaioni; S. Costanzi; R. Volpini; G. Cristalli |
| 591-592 | A Novel and Enantioselective Approach to the Synthesis of Cyclohexane Carbocyclic Nucleosides Starting from (-)-Carvone | Jing Wang; Piet Herdewijn |
| 593-594 | Enantioselective Synthesis and Conformational Analysis of Cyclohexene Carbocyclic Nucleosides | Jing Wang; Piet Herdewijn |
| 595-596 | Design and Biological Evaluation of New Mechanismbased Inhibitors of S-Adenosyl-L-homocysteine Hydrolase | Stanislaw F. Wnuk; Chong-Sheng Yuan; Ronald T. Borchardt; J. Robins Morris |
| 597-598 | Methylenecyclopropane Analogues of Nucleosides: Synthesis, Absolute Configuration, and Enantioselectivity of Antiviral Effect of (R)-(-)- and (S)-( )-Synadenol | Y-L. Qiu; A. Hempel; N. Camerman; A. Camerman; F. Geiser; R. G. Ptak; J. M. Breitenbach; T. Kira; L. Li; E. Gullen; Y-C. Cheng; J. C. Drach; J. Zemlicka |
| 599-600 | Synthesis of 5′-Thioalkyl, Sulfoxide and Sulfone Pyrimidine Nucleosides | L. A. Agrofoglio; F. Girard; F. Fleury; S. Léonce |
| 601-602 | Stereoselective Synthesis of Carbocyclic α-L-Homonucleosides | L. A. Agrofoglio; F. Girard; C. Demaison; M-G. Lee; P. Roingeard; A. Fridland |
| 603-604 | Efficient Stereoselective Synthesis of New C-Nucleosides via Intramolecular Mitsunobu Cyclization | R. Benhida; D. Guianvarch; J-L. Fourrey; J. S. Sun |
| 605-606 | Synthesis of Non-Natural Pyrimidine Nucleosides | Stephanie Blanalt-feidt; Svetlana O. Doronina; Jean-Paul Behr |
| 607-609 | A New and Convenient Approach for the Synthesis of Ribo- and 2′-Deoxyribo-β-L-Furanonucleosides Starting From β-L-Xylofuranonucleosides | V. Boudou; G. Gosselin; J-L. Imbach |
| 835-836 | Investigations into Biochemical Mode of Inhibition of Guanase by Azepinomycin: Synthesis and Biochemical Screening of Several Analogues of Azepinomycin | Vasanthakumar P. Rajappan; Ramachandra S. Hosmane |
| 837-838 | Potent Anti-hepatitis B Viral Activity and Inhibition of Bacteriophage T7 RNA Polymerase by a “Fat” Nucleoside and Its 5′-Triphosphate Derivative: Synthetic, Biochemical, and Biological Studies of 4,8-Diamino-6-imino-6h-1-β-D-ribofuranosylimidazo[4,5-E][1,3]diazepine-5′-triphosphate | Maria Bretner; Dorothy Beckett; Ramachandra S. Hosmane |
| 839-842 | Enzymatic Preparation of 32P-Labeled β-L-2′, 3′-dd-5′ ATP and Its Use as a High-Affinity, Conformation-Specific Ligand for Labeling Adenylyl Cyclases | Roger A. Johnson; Ilana Shoshani; Carmen Dessauer; Gilles Gosselin |
| 843-844 | A New Look at the Molecular Mechanism of Thymidylate Synthase and Its Interaction with Nucleotide Analogues | T. I. Kalman; D. A. Matthews |
| 845-846 | Mechanistic Similarities Between Thymidylate Synthase and IMP Dehydrogenase: A Common Strategy of Catalysis | T. I. Kalman |
| 847-848 | Mechanism of Inhibition of HIV Reverse Transcriptase by 1-(2-Deoxy-β-d-ribofuranosyl)-4-acetylimidazolin-2-one (Imidine) | T. I. Kalman; K. Sen; X-J. Jiang |
| 849-851 | Effect of Acyclic Nucleoside Phosphonates on the HIV-1 Integrase in Vitro | G. Abu Sheika; E. Tramontano; A. G. Loi; P. Franchetti; M. Grifantini; P. La Colla |
| 853-855 | Pyrimidine Nucleotidases/Phosphotransferases from Human Erythrocyte | A. Amici; M. Emanuelli; N. Raffaelli; S. Ruggieri; G. Magni |
| 857-860 | Derivatives of L-Adenosine and L-Guanosine as Substrates for Human Deoxycytidine Kinase | G. Gaubert; G. Gosselin; J-L. Imbach; S. Eriksson; G. Maury |
| 861-862 | On The Catalytic Mechanism of Adenosylhomocysteine/Methylthioadenosine Nucleosidase From E. coli. | Brigitte Allart; Danielle Guillerm; Georges Guillerm |
| 863-864 | Reasons and Limits of Substrate Activity of Modified L-dNTP in DNA Biosynthesis | Alexander A. Krayevsky; Natalya B. Dyatkina; Dmitry G. Semizarov; Liubov S. Victorova; Elena A. Shirokova; Fritz Theil; Martin Von Janta Lipinski; Gilles Gosselin; Jean-Louis Imbach |
| 865-866 | Investigation of the Ternary Complex Formed Between Recombinant Rat Hepatoma Thymidylate Synthase, FdUMP op S4FdUMP and N5, N10-Methylenetetrahydrofolate with the Use of 1H AND 19F NMR | W. Szeszkowski; J. Cieśla; R. Stolarski; W. Rode; T. Kulikowski |
| 867-869 | Interaction of β-L-Adenosine-5′-triphosphate (L-ATP) with Human Deoxycytidine Kinase, Human DNA Primase and T4 DNA Ligase: Does the Chance Direct Enzymatic Enantioselectivity? | A. Verri; A. Montecucco; G. Gosselin; V. Boudou; S. Spadari; J-L. Imbach; F. Focher |
| 871-872 | Binding of Substrates by Purine Nucleoside Phosphorylase (PNP) from Cellulomonas Sp. - Kinetic and Spectrofluorimetric Studies | B. Wielgus-kutrowska; J. Tebbe; J. Wierzchowski; D. Shugar; W. Saenger; G. Koellner; A. Bzowska |
| 873-874 | Synthesis of 2-Chloro-6-aryloxy- and 2-Chloro-6-alkoxyarylpurines and Their Properties in the Purine Nucleoside Phosphorylase (PNP) System | A. Bzowska; L. Magnowska; B. Wielgus-kutrowska; Z. Kazimierczuk |
| 875-876 | Interactions of Calf Spleen Purine Nucleoside Phosphorylase with Antiviral Acyclic Nucleoside Phosphonate Inhibitors: Kinetics and Emission Studies | J. Wierzchowski; E. Kulikowska; A. Bzowska; A. Holy; L. Magnowska; D. Shugar |
| 877-878 | Cell Specific Cytotoxicity and Structure-Activity Relationship of Lipophilic 1-B-D-Arabinofuranosylcytosine (Ara-C) Derivatives | G. J. Peters; D. A. Voorn; C. M. Kuiper; C. Van Der Wilt; P. Noordhuis; K. Smid; F. Myhren; M. Sandvold; H. R. Hendriks |
| 879-880 | Synthesis and Biological Evaluation of Polyaminated 2′,3′-Dideoxy-3′-thiacytidine Prodrugs | M. Camplo; N. Mourier; J-C Chermann; J-L Kraus |
| 881-882 | New Polyazamacrocycle-Nucleoside Conjugates: Synthesis, Anti-HIV Evaluation and Interaction with CXCR-4 Coreceptor | Jean Dessolin; Pascale Galéa; Patrick Vlieghe; Jean-Claude Chermann; Jean-Louis Kraus |
| 883-884 | Synthesis of Novel C-5 Substituted d4t Analogues Bearing Linker Arms as Potential Anti-HIV Agents | D. Ladurée; C. Fossey; M. Renoud-grappin; G. Fontaine; F. Camara; D. Gavriliu; A. Ciurea; A. M. Aubertin; A. Kirn |
| 885-889 | L-Purine Nucleosides as Selective Antimalarials | Annette M. Gero; Gabriel Perrone; David M. Brown; Simone T. Hall; Chung K. Chu |
| 891-892 | Anti-HIV-1 Activities of 1,3-Dioxolane Guanine and 2,6-Diaminopurine Dioxolane | Zhengxian Gu; Mark A. Wainberg; Paul Nguyen-ba; Lucille L'Heureux; Jean-Marc De Muys; Robert F. Rando |
| 893-896 | Quantification of Lamivudine (3TC) by Competitive Immunoassay | Fatima Akeb; Christophe Creminon; Marie-Claire Nevers; Jacques Grassi; Danièle Duval; Roger Guedj |
| 897-898 | Biological Activity of 1-Deazapurine Nucleosides: Role of Deoxycytidine Kinase? | AM. Bergman; G. Cristalli; S. Vittori; J. Wang; S. Eriksson; Gj Peters |
| 901-906 | Antiviral Activity and Resistance Profile of Phosphazid - A Novel Prodrug of AZT | John Machado; Horacio Salomon; Maureen Oliveira; Christos Tsoukas; Alexander A. Krayevsky; Mark A. Wainberg |
| 907-912 | CycloSal-2′-ara (ribo)-fluoro-2′,3′-dideoxyadenosine Monophosphates—An Effort to Solve the Structure-Activity Relationship of 2′-Fluoro-dda | C. Meier; T. Knispel; V. E. Marquez; E. De Clercq; J. Balzarini |
| 913-919 | Antiviral Nucleoside Drug Delivery via Amino Acid Phosphoramidates | Carston R. Wagner; Shu-Ling Chang; George W. Griesgraber; Heng Song; Edward J. McIntee; Cheryl L. Zimmerman |
| 921-926 | DDC- and 3TC-bis(SATE) Monophosphate Prodrugs Overcome Cellular Resistance Mechanisms to HIV-1 Associated with Cytidine Kinase Deficiency | B. Gröschel; N. Himmel; J. Cinatl; C. Périgaud; G. Gosselin; J-L. Imbach; H. W. Doerr; J. Cinatl Jr. |
| 927-932 | Novel Mycophenolic Adenine bis(Phosphonate)S as Potent Anticancer Agents and Inducers of Cells Differentiation | Krzysztof W. Pankiewicz; Krystyna Lesiak-watanabe |
| 933-936 | Effects of cycloSal-D4TMP Derivatives in H9 Cells with Induced AZT Resistance Phenotype | B. Gröschel; C. Meier; R. Zehner; J. Cinatl; H. W. Doerr; J. Cinatl Jr. |
| 937-938 | Aryl Nucleoside H-Phosphonates—Novel Derivatives of Controlled Reactivity | J. Cieślak; J. Jankowska; M. Szymczak; A. Kers; I. Kers; J. Stawiński; A. Kraszewski |
| 939-940 | Synthesis of Analogues of 5′-Mono-,5′-Di-, and 5′-Triphosphate-AZT for the Development of Specific Enzyme Immunoassay for Monitoring of Intracellular Levels of AZT-MP, AZT-DP, and AZT-TP | T. Brossette; M-C. Nevers; C. Creminon; C. Mioskowski; J. Grassi; L. Lebeau |
| 941-942 | Phosphoramidite Chemistry for the Synthesis of cycloSal-Pro-Nucleotides | Florence Mugnier; Chris Meier |
| 943-944 | Evidence for Cyclophosphate Formation During Hydrolysis of 3-Methyl-cycloSal-PCVMP | Andreas Lomp; Chris Meier; Markus Herderich; Peter Wutzler |
| 945-946 | N,O-Selectivity in the Synthesis of 3-Me-CycloSal-ddAMP | Tina Knispel; Chris Meier |
| 947-948 | A New Cyclic Phosphoramidate D4T Prodrug Approach cycloAmb-D4T-Phosphoramidates | Martina Lorey; Chris Meier |
| 949-950 | Synthesis, In Vitro Anti-HIV and Anti-hepatitis B Activities and Pharmacokinetic Properties of Amphiphilic Heterodinucleoside Phosphates Containing ddC and AZT | R. A. Schwendener; P. A. Peghini; P. S. Ludwig; H. Schott |
| 951-953 | Synthesis of Nucleoside 3′-Thiophosphates in One Step Procedure | Maciej B. Szczepanik; Laurent Désaubry; Roger A. Johnson |
| 955-958 | Anti-inflammatory Effects of Phosphonomethoxyethyl Analogues of Adenine in a Model of Adjuvant Arthritis | D. Franková; Z. Zidek; E. Buchar; Z. Jiøièka; A. Holý |
| 959-961 | Stimulation of Cytokine and Nitric Oxide Production by Acyclic Nucleoside Phosphonates | Z. Zídek; D. Franková; A. Holý |
| 963-964 | 2′-Deoxynucleoside 5′-Triphosphates with Reporter Groups Modified at α-, β,γ- or γ-Phosphates as Substrates for DNA Polymerases | L. A. Alexandrova; A. Yu. Skoblov; M. V. Jasko; A. A. Murabuldayev; L. S. Victorova; A. A. Krayevsky |
| 965-966 | Reinvestigation of 4-Thiothymidine-5′-triphosphate Synthesis | H. Bazin; S. Sauvaigo |
| 967-969 | An In Situ Pig Liver Esterase Assay as a Useful Predictive Tool for the Likely In Vitro Anti Viral Activity of Phosphoramidate Pro-Drugs | Carlo Ballatore; Christopher McGuigan; Erik De Clercq; Jan Balzarini |
| 971-972 | Prodrugs of Ara-CMP and Ara-AMP with a S-Acyl-2-thioethyl (SATE) Biolabile Phosphate Protecting Group: Synthesis and Biological Evaluation | R. Bazzanini; S. Manfredini; E. Durini; B. Gröschel; J. Cinatl; J. Balzarini; E. De Clercq; J-L. Imbach; C. Périgaud; G. Gosselin |
| 973-975 | Anti-HIV Pronucleotides: SATE Versus Phenyl as a Protecting Group of AZT Phosphoramidate Derivatives | T. Beltran; D. Egron; I. Lefebvre; C. Périgaud; A. Pompon; G. Gosselin; A-M. Aubertin; J-L. Imbach |
| 977-978 | New Strategies for Chemical Synthesis of Phosphorodithioates Derived from 2′- or 3′- or 5′-Thionucleosides | Izabela Tworowska; Wojciech Dąbkowski |
| 979-980 | Synthesis and Biological Evaluation of Nucleoside Triphosphates Incorporating an Oxyamino Function for “Post-amplification Labelling” | E. Trévisiol; E. Defrancq; J. Lhomme; A. Laayoun; A. Hoang; F. Besème; Ph. Cros |
| 981-982 | Synthesis and Anti-HIV Activity of Some S-Acyl-2-thioethyl (SATE) Phosphoramidate Derivatives of 3′-Azido-2′,3′-dideoxythymidine | D. Egron; C. Périgaud; G. Gosselin; A-M. Aubertin; J-L. Imbach |
| 983-984 | Synthesis, Anti-HIV Activity and Stability Studies of 3′-Azido-2′,3′-dideoxythymidine-5′-fluorophosphate | D. Egron; A. A. Arzumanov; N. B. Dyatkina; A. Krayevsky; J-L. Imbach; A-M. Aubertin; G. Gosselin; C. Périgaud |
| 985-986 | Synthesis of New Acyclic Nucleoside Vinyl Phosphonates | Annamaria Esposito; Maurizio Taddei |
| 987-988 | Intracellular Metabolism of β-L-ddAMP-bis(tbutylSATE), a Potent Inhibitor of Hepatitis B Virus Replication | A. Faraj; L. Placidi; C. Perigaud; E. Cretton-scott; G. Gosselin; L. T. Martin; C. Pierra; R. F. Schinazi; J. L. Imbach; J. P. Sommadossi |
| 989-990 | Synthesis and Biological Application of a New Heterodinucleotide with Both Anti-HSV and Anti-HIV Activity | Palmarisa Franchetti; Ghassan Abu Sheikha; Loredana Cappellacci; Mario Grifantini; Emanuela Balestra; Carlo-Federico Perno; Giorgio Brandi; Luigia Rossi; Mauro Magnani |
| 991-992 | 31P NMR Studies on Oxidative Transformations of Aryl Nucleoside H-Phosphonate Diesters | Annika Kers; Inger Kers; Jacek Cieslak; Adam Kraszewski; Jacek Stawinski |
| 993-994 | Synthesis and In Vitro Antiviral Activity of Some Symmetrical Phosphoramidate Dimers of AZT | I. Kers; J-L. Girardet; G. Gosselin; C. Perigaud; J-L. Imbach; J. Stawinski |
| 995-999 | Synthesis and Transmembrane Transport Studies of Lipophilic Adenosine 5′-Triphosphate Derivatives | Annett Kreimeyer; François André; Aline Bluzat; Catherine Gouyette; Tam Huynh-dinh |
| 1001-1002 | Synthesis of the tBuSATE Pronucleotide of AZT by Two Different Synthetic Approaches | M. Lannuzel; D. Egron; J. -L. Imbach; G. Gosselin; C. Périgaud |
| 1003-1004 | Synthesis of New PMEA Diphosphate Mimics | W. H. G. Laux; C. Périgaud; J. -L. Imbach; G. Gosselin |
| 1005-1006 | Comparison of Anti-HBV Activity of β-D- and β-L-ddA-5′Monophosphate Prodrugs and Effectiveness in Combination with Lamivudine | A. G. Loi; A. Faraj; C. Pierra; G. Gosselin; J. L. Imbach; S. A. Locarnini; E. V. Groman; R. F. Schinazi; J. P. Sommadossi |
| 1007-1008 | Synthesis, Cytostatic Activity and Inhibition of Ribonucleotide Reductase by 5′-Phosphoramidates and 5′-Diphosphates, of 2′-O-Allyl-arabinofuranosyl Nucleosides | S. Manfredini; P. G. Baraldi; E. Durini; J. Balzarini; E. De Clercq; A. Karlsson; V. Buzzoni; L. Thelander |
| 1009-1011 | Analysis of DNA Sequencing Reaction Products Made with 7-Halo-7-deaza-2′-deoxyguanosine-5′-triphosphate | Mark G. McDougall; Louis P. Hosta; Shiv Kumar; Carl W. Fuller |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 18, Number 3 | |
| 307-310 | Preparation of 8-Hydroxy-dGTP and 2-Hydroxy-dATP by a Phosphate Transfer Reaction by Nucleoside-Diphosphate Kinase | Hiroyuki Kamiya; Hiroshi Kasai |
| 311-330 | Interaction of the Recombinant Herpes Simplex Virus Type 1 Thymidine Kinase with Thymidine and Aciclovir: A Kinetic Study | Susanna Kussmann-gerber; Christine Wurth; Leonardo Scapozza; Beatrice D. Pilger; Vladimir Pliška; Gerd Folkers |
| 331-335 | An Efficient, Short Synthesis, and Potent Anti-Hepatitis B Viral Activity of a Novel Ring-Expanded Purine Nucleoside Analogue Containing a 5:7-Fused, Planar, Aromatic, Imidazo[4,5-E][1,3]diazepine Ring System | Huan-Ming Chen; Ramesh Sood; Ramachandra S. Hosmane |
| 337-351 | Synthesis, Lipophilicity, and Anti-HIV Activity of a New Brominated Analog of Zidovudine | Marisa Morura; Horacio Salomón; Guillermo Moroni; Mark Wainberg; Margarita C. Brifiñn |
| 353-361 | Synthesis of New Chiral Peptide Nucleic Acid (PNA) Monomers by a Simplified Reductive Animation Method | Bogdan Falkiewicz; Katarzyna Kowalska; Aleksandra S. Kolodziejczyk; Kazimierz Wiśniewski; Leszek łankiewicz |
| 363-376 | Synthesis of a Novel C-Nucleoside, 2-Amino-7-(2-deoxy-β- D-erythro-pentofuranosyl)-3H,5H-pyrrolo-[3,2-d]pyrimidin-4-one (2′-Deoxy-9-deazaguanosine) | Eric S. Gibson; Krystyna Lesiak; Kyoichi A. Watanabe; Lorraine J. Gudas; Krzysztof W. Pankiewicz |
| 377-391 | Expanding the Catalytic Repertoire of Nucleic Acid Catalysts: Simultaneous Incorporation of Two Modified Deoxyribonucleoside Triphosphates Bearing Ammonium and Imidazolyl Functionalities | David M. Perrin; Thérèse Garestier; Claude Hélène |
| 393-401 | Synthesis of a Monocharged Peptide Nucleic Acid (PNA) Analog and Its Recognition as Substrate by DNA Polymerases | M. J. Lutz; D. W. Will; G. Breipohl; S. A. Benner; E. Uhlmann |
| 403-410 | Recognition of 2′-Deoxyisoinosine Triphosphate by the Klenow Fragment of DNA Polymerase I | Jean-Jacques Beaussire; Sylvie Pochet |
| 411-423 | Molecular Dynamics of Labeled Oligonucleotide Probes Used for the Detection of Point Mutations in DNA | S. Winter; S. Kirschstein; D. P. Millar |
| 425-441 | 7-Deaza-2′-deoxyinosine: A Stable Nucleoside with the Ambiguous Base Pairing Properties of 2′-Deoxyinosine | Frank Seela; Cathrin Mittelbach |
| 443-456 | Chiral Synthons for CARBA-β-D-Ribonucleosides. Synthesis of CARBA-4-Deoxypyrazofurin and Isomeric CARBA-4-Deaza-oxoformycin Analogues | Barbara Mohar; Jože Kobe |
| 457-467 | Novel Triazole 2′-Deoxy-4′-thionucleosides: Stereoselective Synthesis and Biological Evaluation | G. Inguaggiato; M. Jasamai; J. E. Smith; M. Slater; C. Simons |
| 469-474 | Oligonucleotides Quality Control Analysis in Free Solution by Capillary Electrophoresis at Acidic pH | Maria Flora Mangano; Cristina Battaglia; Giuliana Salani; Luigi Rossi Bernardi; Gianluca De Bellis |
| 475-483 | Oligodeoxyribonucleotide Phosphorothioates: Substantial Reduction of (N-1)-mer Content Through the Use of Trimeric Phosphoramidite Synthons | Alessandra Eleuteri; Daniel C. Capaldi; Douglas L. Cole; Vasulinga T. Ravikumar |
| 485-492 | Use of Phenylacetyl Disulfide (PADS) in the Synthesis of Oligodeoxyribonucleotide Phosphorothioates | Zacharia S. Cheruvallath; Patrick D. Wheeler; Douglas L. Cole; Vasulinga T. Ravikumar |
| 493-508 | Synthesis of DNA-(3′)-PNA Chimeras with Conformationally Restricted Linkers Based on 4-Hydroxyproline | Jeroen C. Verheijen; Anne-Marie van Roon; Alexander van der Laan; Gijsbert van der Marel; Jacques van Boom |
| vii-viii | Contributors to this Issue | |
| 2165-2173 | Synthesis and Anti-HSV-1 Activity of 6 Substituted Pyrazolo[3,4-d]Pyridazin-7-one Nucleosides | P. G. Baraldi; S. Manfredini; R. Romagnoli; L. Stevanato; A. N. Zaid; R. Manservigi |
| 2175-2187 | A Synthetic Approach to Carbocyclic Sinefungin | Adilson D. Da Silva; Edmilson JoseMaria; Pierre Blanchard; Jean-Louis Fourrey; Malka Robert-Gero |
| 2189-2197 | A Monoclonal Antibody that Specifically Recognizes m'A Nucleoside | Ruth Espuny; Anna Castro; Carles Codony; Ramon Eritja; Montserrat Bach-Elias |
| 2199-2210 | Detailed Studies on Trimethylselyl Triflate Mediated Glycosylation via a 3,5-O-(l,l,3,3-Tetraisopropyl-Disiloxane-l,3-diyl)-2-O-methylribofuranos-l-yl Trichloroacetimidate Intermediate | Koh-ichiroh Shohda; Takeshi Wada; Mitsuo Sekine |
| 2211-2220 | Crystal Structure and Molecular Conformation of 4-Thiouracil-2′-Trifluorothioacetamide -3′, 5′-Diacetyl-β-D-Riboside | Thamarapu. Srikrishnan |
| 2221-2239 | Synthesis of 4′-Trifluoromethyl Nucleoside Analogs | Janusz Kozak; Carl R. Johnson |
| 2241-2247 | Some Aspects on Acyclonucleoside Synthesis | Masaru Ubasawa; Hideaki Takashima; Kouichi Sdciya |
| 2249-2254 | The Synthesis of 2′-Deoxy-L-Cytidine-3′-Phosphate | Igor A. Kozlov; Leslie E. Orgel |
| 2255-2266 | Quinolone Nucleosides: 6,7-Dihalo-N-β- and α-Glycosyl-l 4-dihydro-4-oxo-quinoline-3-carboxylic Acids and Derivatives. Synthesis, Antimicrobial and Antiviral Activity | Najim A. Al-Masoudi; Yaseen A. Al-Soud; Micheal Ehrmann; Erik de Clercq |
| 2267-2280 | 3′-Deoxy-3′-C-trifluoromethyl Nucleosides: Synthesis and Antiviral Evaluation | S. Lavaire; R. Plantier-Royon; C. Portella; M. de Monte; A. Kirn; A. -M. Aubertin |
| 2281-2288 | The Synthesis of RNA Containing the Modified Nucleotides N2-Methylguanosine and N6, N6-Dimethyladenosine | Jason P. Rife; Charles S. Cheng; Peter B. Moore; Scott A. Strobel |
| 2289-2310 | Synthesis and Antiviral Evaluation of 2′-Deoxy-4′-thio-L-nucleosides and Their Phosphotriester Derivatives Bearing S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups | F. De Valette; J. -L. Barascut; J. -L. Imbach |
| 2311-2322 | Extension of the Applicability of δJ-Values for the Configurational Assignment of Diastereomeric Phosphate-Modified Dideoxynucleotides | Daisy Machytka; Eszter Gács-Baitz; Zsuzsa Tegyey |
| 2323-2333 | 2-Bromoadenosine-Substituted 2′,5′-Oligoadenylates Modulate Binding and Activation Abilities of Human Recombinant RNase L | Yukio Kitade; Masaharu Wakana; Shin-ichi Terai; Takayuki Tsuboi; Masayuki Nakanishi; Chizuko Yatome; Beihua Dong; Robert H. Silverman; Paul F. Torrence |
| 2335-2338 | Improved Deproteciton Procedure for DPSE Protected Phosphorothioates | Achim H. Krotz; Zacharia S. Cheruvallath; Douglas L. Cole; Vasulinga T. Ravikumar |
| 2339-2350 | Synthesis of Peptidinol Adenylates | Annett Kreimeyer; Philippe Marliere |
| 2351-2365 | Improved Targeting of the Flanks of a DNA Stem Using α-Oligodeoxynucleotides.-The Enhanced Effect of an Intercalator | Ahmed F. Khattab; Erik B. Pedersen |
| 2367-2382 | Synthesis of 5-Halogeno-6-amino-2′-deoxyurldines and their Analogs as Potential Inhibitors of Thymidine Phosphorylase | Bai-Chuan Pan; Zhi-Hao Chen; Edward Chu; Ming-Yu WangChu; Shih-Hsi Chu |
| iii-iv | Contributors to this Issue | |
| 1299-1308 | Activation of c-jun and c-fos Genes in dNTP Imbalance Cell Death Induced With 5-Fluoro-2′-Deoxyuridine in Mouse Mammary Tumor FM3A Cell Line | Toshifumi Kakutani; Yoko Ebara; Kae Kanja; Kazushige Takahashi; Yusuke Wataya |
| 1309-1317 | The Characterization of Cell Death Induced by 1-(3-C-Ethynyl-β-D-ribo-Pentofuranosyl)Cytosine (ECyd) in FM3A Cells | Satoshi Takatori; Shinji Tsutsumi; Muneaki Hidaka; Hiroshi Kanda; Akira Matsuda; Masakazu Fukushima; Yusuke Wataya |
| 1319-1324 | As-Triazine Derivatives with Potential Therapeutic Action. XXVI.1 Synthesis of 5-Substituted-6-Azauracil Acyclonucleosides | Carol Cristescu; Francisc Czobor |
| 1325-1331 | Effects of 3′-C-Methylation on the Hydrolytic Stability and Hydroxyl pKa Values of Dinucleoside 2′,5′- and 3′,5′-Monophosphates | Mikko Oivanen; Ekaterina V. Efimtseva; Sergey N. Mikhailov |
| 1333-1345 | A Convenient Synthesis of Acyclic Adenosines with an Unsaturated Side Chain by Modification of 9-(2,3-O-Isopropylidene-D-Ribityl)Adenine | Kosaku Hirota; Yasunari Monguchi; Hironao Sajiki; Chizuko Yatome; Akio Hiraoka; Yukio Kitade |
| 1347-1353 | New Approach to the Solid Phase Synthesis of N3′→P5′ Phosphoramidate Oligonucleotides | Janina Baraniak; Dariusz Korczyński; Renata Kaczmarek; Ewa Wasilewska |
| 1355-1363 | Synthesis of 1-(β-D-Glycopyranosyl)-3-Deazapyrimidines from 2-Hydroxy and 2-Mercaptopyridines | Adel M. Attia; Galal H. Elgemeie; Ibrahim S. Alnaimi |
| 1365-1372 | Synthesis and Reactions of Some 3′,4′-Unsaturated 2′,3′-Secouridine Analogues | Shinya KIKUCHI; Tomohiro MAEKAWA; Katsumaro MINAMOTO; Keizo TANIGAWA |
| 1373-1384 | Acyclo C-Nucleoside Analogs. Regioselective Annellation of a Triazole Ring to 5-Methyl-1,2,4-Triazino[5,6-b]Indole and Formation of Certain 3-Poly Hydroxyalkyl Derivatives | Nagwa Rashed; Hamida Abdel Hamid; El Sayed Ramadan; El Sayed H. El Ashry |
| 1385-1407 | Synthesis of Acyclo C-Nucleosides OF Phenanthro[9,10-e][1,2,4]Triazino[3,4-c]-[1,2,4] Triazoles, and Their Precursors | Atef Hamed; Elham R. Abo-Amaym; El Sayed H. El Ashry |
| 1409-1443 | Synthesis and Antiviral Evaluation of Analogs of Adenosine-N1-Oxide and 1-(Benzyloxy)Adenosine | Cecil D. Kwong; Charles A. Krauth; Anita T. Shortnacy-Fowler; Gussie Arnett; Melinda G. Hollingshead; William M. Shannon; John A. Montgomery; John A. Secrist III |
| 1445-1451 | A New Regio-Defined Synthesis of PMEA | Qun Dang; Van Liu; Mark D. Erion |
| 1453-1471 | Synthesis of γ-Phosphate-Linked Nucleoside Affinity Chromatography Resins for Protein Purification, Including Ribonucleoside Triphosphate Reductase | Robert K. Suto; Martin A. Whalen; Bruce R. Bender; Richard G. Finke |
| 1473-1487 | Synthesis and Antiviral Activity of Apio Dideoxy Nucleosides with Azido or Amino Substituent | Lak Shin Jeong; Young A. Lee; Hyung Ryong Moon; Moon Woo Chun |
| 1489-1504 | Potential Antiviral Agents. Part II. Synthesis and Antiviral Evaluation of Pyrazinones Substituted With Acyclic Chains | Jean Davis; Rachida Benhaddou; Olessia Fedoryak; Robert Granet; Pierre Krausz; Christophe Bliard; Michele De Monte; Anne Marie Aubertin |
| 1505-1513 | Synthesis and Biochemical Study of N2-(p-n-Butylphenyl)-2′-deoxyguanosine 5′-(α,β-imido)triphosphate (BuPdGMPNHPP): A Non-Substrate Inhibitor of B Family DNA Polymerases | James M. Stattel; Ivan Yanachkov; George E. Wright |
| 1059-1062 | Synthesis and Anti-HIV Activity of Carbocyclic Ring-Enlarged 4′,1′a-Methano Oxetanocin Analogues | Lak S. Jeong; Min Bae; Moon W. Chun; Victor E. Marquez |
| 1063-1066 | Synthesis of Novel 3′-C-Hydroxymethyl Nucleosides by a Convergent Strategy | Pia Nørregaard Jørgensen; Jesper Wengel |
| 1067-1071 | Synthesis of the Sulfonylpyrimidine Derivatives as a New Type of Sulfonylcycloureas | Biserka Kašnar; Irena Krizmanić; Mladen Žinić |
| 1073-1077 | Synthesis of 3′-Deoxy-3′ and 5′-Deoxy-5′-[4-(Purin-9-yl/Pyrimidin-1-yl) methyl-1,2,3-Triazol-1-yl]thymidine via 1,3-Dipolar Cycloaddition | H. B. Lazrek; M. Taourirte; T. Oulih; Y. Kabbaj; J. L. Barascut; J. L. Imbach; N. A. Almasoudi; W. Pfleiderer |
| 1079-1082 | Synthesis of N-Arylinosines | Tokumi Maruyama; Yoshiko Sato; Takeshi Goto; Mitsutoshi Fukuhara |
| 1083-1086 | Synthesis and Biological Evaluation of 2′,3′-Dideoxy-3′-Fluororibofuranosyl Purine Nucleosides | Nicolai E. Poopeiko; Natalia B. Khripach; Zygmunt Kazimierczuk; Jan Balzarini; Erik De Clercq; Igor A. Mikhailopulo |
| 1087-1090 | Dinucleotides Incorporating Isomeric Nucleosides: Synthesis, Structural and Stereochemical Characterization, and Enzymology | Tamera S. Jahnke; Qi Chao; Vasu Nair |
| 1091-1094 | Synthesis of New Dideoxynucleosides Bearing Ring-Extended Nucleobases | Jianzhong Zhang; Vasu Nair |
| 1095-1097 | Novel Intramolecular Introduction of Nucleophiles To 2,2′-Anhydrouridine | Danny P. C. McGee; Alecia Vaughn-Settle |
| 1099-1102 | 4-Substituted Uridine 5′-Triphosphates as Agonists of the P2Y2 Purinergic Receptor | Sammy R. Shaver; William Pendergast; Suhaib M. Siddiqi; Benjamin R. Yerxa; Dallas K. Croom; Robert W. Dougherty; Michael K. James; A. Neil Jones; Janet L. Rideout |
| 1103-1106 | Synthesis and Biological Activities of 2′-Modified 4′-Thionucleosides | Yuichi Yoshimura; Kenji Kitano; Mikari Watanabe; Hiroshi Satoh; Shinji Sakata; Shinji Miura; Noriyuki Ashida; Haruhiko Machida; Akira Matsuda |
| 1107-1110 | Addition of 2,3-Dihydrofuran to N2-Acetyl-8-bromoguanine | M. Madre; R. Zhuk; G. -J. Koomen |
| 1111-1114 | Synthesis and Properties of Oligonucleotides Containing 5-Aza-2′-deoxycytidine | Ramon Eritja; Victor E. Marquez; Ramon Güimil García |
| 1115-1118 | Synthesis of New 1,2,3-Triazole Acyclonucleoside Analogues of ACV and HBG | H. B. Lazrek; M. Taourirte; T. Oulih; M. Lebtoumi; J. L. Barascut; J. L. Imbach |
| 1121-1127 | Delivery of Polynucleotides with Polyamine Lipids and Polymers | B. A. Demeneix; O. Boussif; M. A. Zanta; J. S. Remy; J. P. Behr |
| 1129-1138 | Conjugated Antisense Oligonucleotides | Muthiah Manoharan; Kathleen L. Tivel; Thomas P. Condon; Laura K. Andrade; Isabelle Barber-Peoch; Gopal Inamati; Shefali Shah; Venkatraman Mohan; Mark J. Graham; C. Frank Bennett; Stanley T. Crooke; P. Dan Cook |
| 1139-1140 | Cholesterol Conjugated Uniform and Gapmer Phosphorothioate Oligonucleotides Targeted Against PKC-α and C-raf Gene Expression | Muthiah Manoharan; Kathleen L. Tivel; Gopal Inamati; Brett P. Monia; Nick Dean; P. Dan Cook |
| 1141-1143 | 2′- and 3′- Cholesterol-Conjugated Adenosine and Cytosine Nucleoside Building Blocks: Synthesis of Lipidic Nucleic Acids | Muthiah Manoharan; Gopal Inamati; Kathleen L. Tivel; Boyd Conklin; Bruce S. Ross; P. Dan Cook |
| 1145-1153 | Preclinical Profiling of Modified Oligonucleotides: Anticoagulation and Pharmacokinetic Properties | Paul L. Nicklin; John Ambler; Andrew Mitchelson; Deborah Bayley; Judy A. Phillips; Sarah J. Craig; Brett P. Mania |
| 1155-1163 | Enhanced Antisense Effects Resulting from an Improved Streptolysin-O Protocol for Oligodeoxynucleotide Delivery into Human Leukaemia Cells | R. V. Giles; J. Grzybowski; D. G. Spiller; D. M. Tidd |
| 1165-1168 | Modification of a Phosphorothioate Oligonucleotide with Cholesterol Induces Association of the Oligonucleotide to Serum Lipoproteins and Affects Its Biological Fate | Martin K. Bijsterbosch; Muthiah Manoharan; Kathleen L. Tivel; Erik T. Rump; Erik A. L. Biessen; Remco L. A. De Vrueh; P. Dan Cook; Theo J. C. van Berkel |
| 1169-1172 | Conjugated Antisense Oligonucleotides for Inhibition of Human Cytomegalovirus In Vitro | Zhaoda Zhang; Jean A. Smith; Adrienne P. Smyth; Warren Eisenberg; Alexandra Nichols; Gregory S. Pari; Jin Yan Tang |
| 1173-1182 | Restoration of ß-Globin Gene Expression in Mammalian Cells by Antisense Oligonucleotides That Modify the Aberrant Splicing Patierns of Thalassemic Pre-mRNAs | Halina Sierakowska; Michael Montague; Sudhir Agrawal; Ryszard Kole |
| 1183-1194 | Targeted Gene Correction: Synthesis and Characterization of Double-Hairpin 2′-O-Methyl RNA/DNA Chimera Oligonucleotides | Alex Andrus; Ravi Vinayak; Robert G. Kuimelis; Bashar Mullah |
| 1195-1199 | Inhibition of 5-α-Reductase (TYPE-II) Expression by Antisense 3′-Deoxy-(2′-5′) Oligonucleotide Chimeras | Purshotam Bhan; Anila Bhan; Mikung Hong; John G. Hartwell; June M. Saunders; Glenn D. Hoke |
| 1201-1204 | Synthesis of (2′,5′)-Oligoadenylate Antisense Chimeras Targeting Steroid 5α-Reductase | Hagen Cramer; Paul F. Terrence |
| 1205-1208 | Biologically Active Oligodeoxyribonucleotides. VII. Anti-HIV-1 Activity of Hexadeoxyribonucleotides Bearing 3′- and 5′-End-Modifications | Makoto Koizumi; Rika Koga; Hitoshi Hotoda; Kenji Momota; Toshinori Ohmine; Hidehiko Furukawa; Takashi Nishigakit; Koji Abe; Toshiyuki Kosaka; Masakatsu Kaneko; Satoshi Kimura; Kaoru Shimada |
| 1209-1212 | Synthesis of 3′,5′-Dithymidylyl-α-hydroxyphosphonate Dimer Building Blocks for Oligonucleotide Synthesis—A New Pro-oliguncleotide | Ralf P. Mauritz; Chris Meier; Eugen Uhlmann |
| 1213-1214 | The Pro-Oligonucleotide Approach: Chimeric Dodecamers Bearing Six Bioreversible Protecting Groups | F. Morvan; G. Tosquellas; N. Mignet; I. Barber; B. Rayner; J. -L. Imbach |
| 1215-1219 | Enhanced Specificity of Minimally Modified Anti-c-myc Oligonucleotides | A. Peyman; H. Ragg; T. Ulshöfer; D. W. Will; E. Uhlmann |
| 1221-1222 | Targeting HIV mRNA for Degradation: 2,5-A Antisense Chimeras as Potential Chemotherapeutic Agents for AIDS | Mark R. Player; Ratan Maitra; Robert Silverman; Paul F. Torrence |
| 1223-1226 | Conjugation of Oligonucleotides with Steroid Structures and Their Interaction with the Low-Density Lipoprotein | Erik T. Rump; Remco L. A. de Vrueh; Erik A. L. Biessen; Theo J. C. van Berkel; Martin K. Bijsterbosch |
| 1229-1233 | Beta-L-(-)-dioxolane Cytidine (β-L-(-)-OddC) as a Potent Compound for the Treatment of Cancer | K. L. Grove; X. Guo; S-H. Liu; M. Kukhanova; C-K. Chu; Y-C. Cheng |
| 1235-1240 | Resistance Profile of a Novel 2′, 3′ - Dideoxynucleoside Analog with Activity Against HIV-1 | Nathalie Richard; Antonietta R. Belmonte; Horacio Salomon; Kazushige Nagai; Tarek Mansour; Mark A. Wainberg |
| 1241-1249 | Characterization of GPI2A, a Potent Inhibitor of HIV-1 Gene Expression and Viral Replication | Michael I. Anazodo; Elena Duta; Horacio Salomon; Albert D. Friesen; Mark A. Wainberg; Jim A. Wright |
| 1251-1259 | Suicide Gene Therapy for Intrinsically Drug Resistant Solid Tumors | J. Arly Nelson; Bih-Fang Pan; Frank C. Marini III; David Farquhar; Craig A. Mullen |
| 1261-1270 | Gemcitabine: Actions and Interactions | William Plunkett; Peng Huang; Varsha Gandhi |
| 1271-1278 | Modulation of DNA Triplex Stability Through Nucleobase Modifications | Krishna N. Ganesh; Kallanthottathil G. Rajeev; Pradeep S. Pallan; Vipul S. Rana; Dinesh A. Barawkar; Vaijayanti A. Kumar |
| 1279-1282 | Lipophilic Derivatization of the Antiviral Drug 9-(2-Phosphonylmethoxyethyl)adenine and Its Incorporation into a Lactosylated Lipid Carrier to Improve Its Liver Uptake | Remco L. A. de Vrueh; Erik T. Rump; Erik A. L. Biessen; Jan Balzarini; Theo J. C. van Berkel; Martin K. Bijsterbosch |
| 1283-1286 | Comparison of the Inhlbitory Effects of 2-Chloro-2′-deoxyadenosine and 9-β-D-Arabinosyl-2-fluoro-adenine on Metabolism of Deoxyadenosine in Human Lymphocytes and Erythrocytes | Krystyna Fabianowska-Majewska; Dorota Wyczechowska |
| 1287-1290 | Antiviral Activities of β-Enantiomers of 3′-Substituted-3′-deoxythymidine Analogs | Abdesslem Faraj; M. Abdelaziz El Alaoui; Geraldine Pavia; Gilles Gosselin; Jean-Louis Imbach; Raymond F. Schinazi; Jean Pierre Sommadossi |
| 1291-1294 | Anti-Inflammatory Activity of Purine Nucleoside Analogs | Stephanie A. Hartsel; Cecil Chen; John Kennedy; Allison Bendele; Cliff Wright; William S. Marshall |
| 1295-1299 | Thiated Pyrimidine Deoxynucleoside Analogues, Potential Chemotherapeutic Agents, and Substrates/Inhibitors in Various Enzyme Systems | M. Bretner; K. Felczak; J. M. Dzik; B. Golos; W. Rode; A. Drabikowska; J. Poznanski; K. Krawiec; A. Piasek; D. Shugar; T. Kulikowski |
| 1301-1302 | Derivatives of Imidazole-4-carboxamide as Substrates for Various DNA Polymerases | Christine Le Bec; Pascal Roux; Henri Buc; Sylvie Pochet |
| 1303-1306 | Cyclo-saligenyl-2′,3′-dideoxy-2′,3′-didehydroythymidinemonophosphate (cycloSal-d4TMP) — A New Pro-Nucleotide Approach | Chris Meier; Martina Lorey; Eric De Clercq; Jan Balzarini |
| 1307-1310 | Cyclo-saligenyl-5-fluoro-2′-deoxyuridinemonophosphate (cycloSal-FdUMP) — A New Prodrug Approach for FdUMP | Martina Lorey; Chris Meier; Eric De Clercq; Jan Balzarini |
| 1311-1314 | Di-ddU-α-Hydroxyphosphonate and α-Hydroxy- α- METHYLPHOSPHONATES as Potential Prodrugs of Antiviral Nucleoside Analogues | Lothar W. Habel; Chris Meier |
| 1315-1319 | Synergistic Combinations of Nucleoside Analog Drugs with Other Drugs Induce Greater Apoptosis in Human Leukemic T-Cells | Partha Nandy; Antonia P. Periclou; Vassilios I. Avramis |
| 1321-1324 | The Pronucleotide Approach. I. Synthesis, Anti-HIV Activity and Preliminary Stability Studies of Mononucleoside S,S′-Bis(O-acyl-2-oxyethyl) Phosphorodithiolates | N. Schlienger; C. Périgaud; G. Gosselin; I. Lefebvre; A. Pompon; A. -M. Aubertin; A. Kirn; J. -L. Imbach |
| 1325-1329 | The Pronucleotide Approach. II: Synthesis and Preliminary Stability Studies of Mononucleoside Glycosyl Phosphotriester Derivatives | N. Schlienger; C. Périgaud; G. Gosselin; J. -L. Imbach |
| 1331-1335 | The Pronucleotide Approach. III. Synthesis, Anti-HBV Activity and Stability Studies of the Bis(S-pivaloyl-2-thioethyl) Phosphotriester Derivative of Acyclovir | Gilles Valette; Jean-Luc Girardet; Alain Pompon; Christian Périgaud; Gilles Gosselin; Brent Korba; Olivier Hantz; Jean-Louis Imbach |
| 1337-1339 | Synthesis and Biological Activity of Some 2-Aminopurine Carbonucleosides | L. Santana; M. Teijeira; E. Uriartea; C. Terán; G. Andrei; R. Snoeck; E. De Clercq |
| 1341-1345 | Phosphodiester Amidates of Unsaturated Nucleoside Analogues as Anti-HIV Agents | Holger Winter; Yosuke Maeda; Hiroaki Mitsuya; Jiri Zemlicka |
| 1347-1350 | Antileukemic Activities and Mechanism of Action of 2′-Deoxy-4′-methylcytidine and Related Nucleosides | Toyofumi Yamaguchi; Aki Tomikawa; Toshiaki Hirai; Takeo Kawaguchi; Hiroshi Ohrui; Mineo Saneyoshi |
| 1351-1354 | Synthesis and Biological Activity of New 2′ 5′-Oligonucleotides | Evgeny I. Kvasyuk; Tamara I. Kulak; Igor A. Mikhailopulo; Robert J. Suhadolnik; Earl E. Henderson; Susan E. Horvath; Ming-Xu Guan; Wolfgang Pfleiderer |
| 1357-1368 | Sequence-Specific Cleavage of RNA Using Macrocyclic Lanthanide Complexes Conjugated to Oligonucleotides: A Structure Activity Study | Jonathan Hall; Dieter Hüsken; Robert Häner |
| 1369-1378 | Pteridine Nucleosides—New Versatile Building Blocks in Oligonucleotide Synthesis | Ramamurthy Charubala; Juris Maurinsh; Angelika Rösler; Manuel Melguizo; Oliver Jungmann; Margarete Gottlieb; Jörg Lehbauer; Mary Hawkins; Wolfgang Pfleiderer |
| 1379-1388 | Potent and Selective Ligands for Adenosine Binding Sites | G. Cristalli; E. Camaioni; E. Di Francesco; A. Eleuteri; S. Vittori; R. Volpini |
| 1389-1398 | New Unnatural L-Nucleoside Enantiomers:From Their Stereospecific Synthesis to Their Biological Activities | G. Gosselin; V. Boudou; J. -F. Griffon; G. Pavia; C. Pierra; J. -L. Imbach; A. -M. Aubertin; R. F. Schinazi; A. Faraj; J. -P. Sommadossi |
| 1399-1402 | Conformational Studies of 3′-Spironucleosides (TSAO-T and Analogues) by NMR Spectroscopy | Rosa Alvarez; María-Luisa Jimeno; Francisco J. Tomás-Gil; María-Jesús Pérez-Pérez; María-José Camarasa |
| 1403-1406 | A Study Towards Total Synthesis of Antibiotic Agrocin 84 | Dmitri Filippov; Cornelis M. Timmers; Gijs A. van der Marel; Jacques H. van Boom |
| 1407-1410 | Solid Phase Conjugation Chemistry: Use of Alloc as a Protecting Group for 2′-Aminolinker Containing Oligonucleotides | Isabelle Barber-Peoc'h; Muthiah Manoharan; P. Dan Cook |
| 1411-1413 | 2′- and 3′- Biotin Conjugated Nucleoside Building Blocks: Synthesis of Biotinylated Oligonucleotides | Muthiah Manoharan; Gopal Inamati; Kathleen L. Tivel; Patrick Wheeler; Kim Stecker; P. Dan Cook |
| 1415-1418 | Synthesis and IMP Dehydrogenase (Type I and Type II) Inhibitory Activity of Isosteric NAD Analogs Derived from Thiophenfurin and Furanfurin | P. Franchetti; L. Cappellacci; G. Abu Sheikha; H. N. Jayaram; B. P. Schneider; T. Sint; V. V. Gurudutt; F. R. Collart; E. Hubeman; M. Grifantini |
| 1419-1421 | Development of Novel Bridged and Caged Nucleoside Analogs as Biochemical Tools | Michael P. Groziak; Ronghui Lin |
| 1423-1426 | 1,5-Translocation Strategy for Nucleoside Anomeric Radicals | Atsushi Kittaka; Hiromichi Tanaka; Naoki Yamada; Hajime Kato; Tadashi Miyasaka |
| 1427-1429 | The Synthesis of Enantiomerically Pure Pyrazolo[4,3-c]pyridine Carbarzbo C-Nucleoside | Barbara Mohar; Jože Kobe |
| 1431-1434 | Conformational Analysis of Nucleosides Constructed on a Bicyclo[3.1.0]hexane Template. Structure-Antiviral Activity Analysis for the Northern and Southern Hemispheres of the Pseudorotational Cycle | Victor E. Marquez; Abdallah Ezzitouni; Maqbool A. Siddiqui; Pamela Russ; Hisafumi Ikeda; Clifford George |
| 1435-1438 | Novel Bicyclic Nucleoside Analogues Related to Natural Griseolic Acids | Lea Pickering; Vasu Nair |
| 1439-1442 | Synthesis and Evaluation of Novel Oligodeoxynucleotides Containing 3′-C-(3-Benzoyloxypropyl)thymidine and Bicyclo Nucleoside Derivatives | Henrik M. Pfundheller; Poul Nielsen; Jesper Wengel |
| 1443-1446 | Properties of Some Diuridine Phosphate Analogues | Bhisma K. Patel; James B. Thomson; Victor Jiménez; Klaus Eckart; Fritz Fxkstein |
| 1447-1451 | Steric and Stereoelectronic Effects of 7-Deazapurine Bases on the Sugar Conformation of 2′-Deoxynucleosides | Helmut Rosemeyer; Natalya Ramzaeva; Matthias Zulauf; Horst Thomas; Yaoming Chen; Cathrin Mittelbach; Frank Seela |
| 1453-1456 | 1,2-Disubstituted Carbocyclic Analogues of Thymine Nucleosides | V. Escuredo; B. Ferro; L. Santana; M. Teijeira; E. Uriarte |
| 1457-1460 | 2′-C-Alkylribonucleosides: Design, Synthesis, and Conformation | Rogers E. Harry-O'kuru; Emily A. Kryjak; Michael S. Wolfe |
| 1461-1464 | New Pyrene Derivatives for Fluorescent Labeling of Oligonucleotides | V. A. Korshun; I. A. Prokhorenko; S. V. Gontarev; M. V. Skorobogatyi; K. V. Balakin; E. V. Manasova; A. D. Malakhov; Yu. A. Berlin |
| 1465-1468 | Synthesis of Circular Oligonucleotide Conjugates | O. G. Chakhmakhcheva; A. A. Buryakova; M. V. Choob; A. L. Kalinkina; V. A. Efimov; R. F. Rando |
| 1469-1472 | Structural Studies of 2-Thiouridine in RNA | Raju K. Kumar; Darrell R. Davis |
| 1473-1474 | Unexpected High Hybridization Properties of α-Anomeric Oligodeoxynucleoside Methylphosphonates | F. Debart-Vasseur; J. -J. Vasseur; J. -L. Imbach; B. Rayner |
| 1475-1480 | Synthesis of Novel DNA Analoues Containing Aminomethylphosphonate Internucleoside Linkages | V. A. Efimov; M. V. Choob; A. L. Kalinkina; O. G. Chakhmakkcheva |
| 1481-1485 | DNA Duplexes Containing Alpha Anomeric Nucleotides and Polarity Reversals: Coexistence of Parallel and Antiparallel DNA | Markus W. Gerrnann; James M. Aramini; Bernd W. Kalisch; Richard T. Pon; Johan H. van de Sande |
| 1487-1488 | Stepwise Solid-Phase Synthesis of Serine-, Tyrosine- and Homoserine-nucleopeptides | Maite Beltrán; Marta Maseda; Yolanda Pérez; Jordi Robles; Enrique Pedroso; Anna Grandas |
| 1489-1490 | Novel DNA Damage Mediated by Oxidation of Various Modified Nucleotide Residues | Hideo Inoue; Shiro Koizume; Takahiro Yamauchi; Kouichi Murata; Eiko Ohtsuka |
| 1491-1495 | Synthesis, Biophysical Properties, and Stability Studies of Mixed Backbone Oligonucleotides Containing Novel Non-Ionic Linkages | Radhakrishnan P. Iyer; Dong Yu; Theresa Devlin; Nan-Hui Ho; Suzanne Johnson; Sudhir Agrawal |
| 1497-1501 | The Synthesis of 2′-C-Functionalised Nucleosides for Incorporation into Catalytic RNA | Anthony J. Lawrence; John B. J. Pavey; Ian A. O'Neil; Richard Cosstick |
| 1503-1505 | Comparison of Physicochemical and Biological Properties of (o-Carboran-1-YL)methylphosphonate and Methylphosphonate Oligonucleotides | Zbipniew J. Lesnikowski; Robert M. Lloyd Jr.; Raymond F. Schinazi |
| 1507-1511 | Properties of Oligonucleotides Containing the Transition Bases P and K | F. Hill; D. Loakes; D. M. Brown |
| 1513-1514 | A Solid-Phase Method for the Synthesis of Small to Medium-Sized Cyclic Oligonucleotides | ElMostafa Alazzouzi; Nuria Escaja; Marcus Straub; Blanca Martí; Anna Grandas; Enrique Pedroso |
| 1515-1518 | A Novel Class of 4′-Aza Analogues of 2′,3′-Dideoxynucleosides as Potential Anti-HIV Drugs | Antonella Leggio; Angelo Liguori; Antonio Procopio; Carlo Siciliano; Giovanni Sindona |
| 1519-1522 | Amino Acid Nucleic Acids: Synthesis and Hybridization Properties of a Novel Class of Antisense Oligonucleotides | Kanda S. Ramasamy; Wilfried Seifert |
| 1523-1527 | Oligonucleotides Containing Consecutive 2′-Deoxy-Isoguanosine Residues: Synthesis, Parallel Duplex Formation and Identification of a d(T4iG4T4) Tetraplex | Frank Seela; Changfu Wei; Alexander Melenewski |
| iii-iv | Contributors to The Issue | |
| v | Editor's Note | |
| 1679-1686 | SYNTHESIS OF CYCLIC DINUCLEOTIDES BY AN H-PHOSPHONATE METHOD IN SOLUTION | Fan Zeng; Roger A. Jones |
| 1687-1700 | 2′-SUBSTITUTED PHOSPHOROTHIOATE CONTAINING OLIGORIBONUCLEOTIDES: AN APPLICATION TO THE SYNTHESIS AND PURIFICATION OF HAMMERHEAD RIBOZYMES | Anthony DiRenzo; Susan Grimm; Kurt Levy; Peter Haeberli; Lara Maloney; Nassim Usman; Francine Wincott |
| 1701-1710 | SYNTHESIS AND STRUCTURE DETERMINATION OF A NUCLEOSIDEDERIVED NEW HETEROCYCLIC SYSTEM: 8H,10H,15b(S)-2,3,6,7-TETRAHYDRO-1,5,3-DIOXAZEPINO[3,2-c]INDOLO[3,2-g]PTERIDINE-7-ONE | Ping Ge; Gregory O. Voronin; Thomas I. Kalman |
| 1711-1718 | PHOSPHONATE ANALOGS OF CARBOCYCLIC PHOSPHORIBOSYLAMINE AND CARBOCYCLIC GLYCINAMIDE RIBONUCLEOTIDE | Robert Vince; Mei Hua; Carol A. Caperelli |
| 1719-1723 | MALDI AND FAB MASS SPECTROMETRY OF NUCLEOSIDE TRIPHOSPHATES: A COMPARATIVE STUDY | Kevin Burgess; David H. Russell; Aroonsiri Shitangkoon; Alex J. Zhang |
| 1725-1739 | PHOSPHONOACETATE DERIVATIVES OF OLIGODEOXYRIBONUCLEOTIDES | M Jonathan Rudolph; Michael S. Reitman; Eric W. MacMillan; Alan F. Cook |
| 1741-1749 | HYDROLYSIS OF 2′-DEOXY AND 2′-FLUORONUCLEOSIDE-3′-PHOSPHODlESTERS | L. Y. Kuo; K. Travers; J. Chock |
| 1751-1769 | SYNTHESIS OF NOVEL BICYCLIC NUCLEOSIDES RELATED TO NATURAL GRISEOLIC ACIDS | Lea Pickering; Vasu Nair |
| 1771-1778 | AN IMPROVED SYNTHESIS OF 9-[2-(DIETHOXYPHOSPHONOMETHOXY)ETHYL]ADENINE AND ITS ANALOGUES WITH OTHER PURINE BASES UTILIZING THE MITSUNOBU REACTION | Wei Chen; Michael T. Flavin; Robert Filler; Ze-Qi Xu |
| 1779-1795 | SYNTHESIS OF PYRAZOLO[4,3-C]PYRIDINE C-RIBONUCLEOSIDES VIA AN EFFECTIVE TETRAZOLE TO PYRAZOLE TRANSFORMATION | Marija Prhavc; Jože Kobe |
| 1797-1803 | REACTION OF ANHYDRONUCLEOSIDES WITH MAGNESIUM ALKOXIDES: REGIOSPECIFIC SYNTHESIS OF 2′-O-ALKYLPYRIMIDINE NUCLEOSIDES. | Danny P. C. McGee; Yansheng Zhai |
| 1805-1819 | CRYSTAL STRUCTURE OF 1,3,5-TRIMETHYL-N4-HYDROXYCYTOSINE, AND ITS RELEVANCE TO THE MECHANISM OF HYDROXYLAMINE MUTAGENESIS | Karin Bjåmer Birnbaum; Borys Kierdaszuk; David Shugar |
| 1821-1834 | SYNTHESES OF 2′,3′-DIDEOXY-D-C-NUCLEOSIDES FROM γ-LACTONE | Yuejun Xiang; Jinfa Du; Chung K. Chu |
| 1835-1847 | SYNTHESIS AND BIOLOGICAL ACTIVITY OF 5-SUBSTITUTED ANTI-CONSTRAINED ACYCLIC ANALOGS OF CYTIDINE AND URIDINE | Ling-Yih Hsu; Ya-Mei Chang; Chung-Hsun Lin; John C. Drach |
| 1849-1861 | SYNTHESIS OF 3-ALKYL PIPERAZIN-2-ONE NUCLEOSIDES WITH POTENTIAL ANTIRETROVIRAL ACTIVITY | Abdellah Benjahad; Robert Granet; Pierre Krausz; Claudine Bosgiraud; Sylvie Delebassée |
| xi-xiv | Contributors to This Issue | |
| xv-xvii | Preface | |
| 1-16 | Ribosylation of the Base Residue of Inosine Derivatives by Phase-Transfer Catalysis | Keiichi Aritomo; Chihiro Urashima; Takeshi Wada; Mitsuo Sekine |
| 17-30 | An Efficient Method for the Synthesis of β-d-Ribonucleosides Catalyzed by Metal Iodides | Teruaki Mukaiyama; Masashi Nagai; Takafumi Matsutani; Naoyuki Shimomura |
| 31-45 | Synthesis of 2′,3′-Dideoxypurinenucleosides via the Palladium Catalyzed Reduction of 9-(2,5-Di-O-acetyl-3-bromo-3-deoxy-β-d-xylofuranosyl)purine Derivatives | Hiroshi Shiragami; Yusuke Amino; Yutaka Honda; Masayuki Arai; Yasuhiro Tanaka; Hisao Iwagami; Toshihide Yukawa; Kunisuke Izawa |
| 47-58 | Synthesis of 1-(2,3-Dideoxy-β-d-glycero-pent-2-enofuranosyl)thymine (d4T; Stavudine) from 5-Methyluridine | Hiroshi Shiragami; Takashi Ineyama; Yumiko Uchida; Kunisuke Izawa |
| 59-68 | Design and Synthesis of Heterocyclic Carboxamides as Natural Nucleic Acid Base Mimics | Donald E. Bergstrom; Peiming Zhang; W. Travis Johnson |
| 69-84 | Synthesis and Conformational Studies of New Purine Isodideoxynucleosides | Lawrence B. Zintek; Tamera S. Jahnke; Vasu Nair |
| 85-96 | Intramolecular Radical Reactions of 5′-O-Modified 2′,3′-Didehydro-2′,3′-Dideoxyuridine Derivatives | Kaoru Hisa; Atsushi Kittaka; Hiromichi Tanaka; Kentaro Yamaguchi; Tadashi Miyasaka |
| 97-107 | Tandem Radical Cyclization-Oxygenation of 6-(2,2-Di-bromovinyl)-1-(2-deoxy-d-erytho-pent-1-enofuranosyl)-uracil: Synthesis of Anomeric Spiro Nucleosides Having Arabino and Ribo Configurations | Atsushi Kittaka; Yasuhiko Tsubaki; Hiromichi Tanaka; Kazuo T. Nakamura; Tadashi Miyasaka |
| 109-119 | Synthesis of the Fluoromethyl Derivatives of Carbocyclic Oxetanocin A | Yoshiko Sato; Kenji Ueyama; Tokumi Maruyama; Douglas D. Richman |
| 121-134 | The Synthesis of Some 5-Alkyl (Cycloalkyl)-Substituted 2′ -Deoxy-4′-Thiouridines | I. Basnak; M. Sun; P. L. Coe; R. T. Walker |
| 135-148 | Some Reactions of 4′-Thionucleosides and Their Sulfones | E. Louise Hancox; Richard T. Walker |
| 149-167 | Synthesis of Methylene-Bridged Analogues of Nicotinamide Riboside, Nicotinamide Mononucleotide and Nicotinamide Adenine Dinucleotide | Pawel Lipka; Andrzej Zatorski; Kyoichi A. Watanabe; Krzysztof W. Pankeiwicz |
| 169-181 | Nucleosides and Nucleotides. 139. Stereoselective Synthesis of (2′S)-2′-C-Alkyl-2′-deoxyuridines | Tomoharu Iino; Satoshi Shuto; Akira Matsuda |
| 183-204 | Synthesis of 2′-C-α-Methyl-2′,3′-dideoxynucleosides | Indrajit Giri; Pascal J. Bolon; Chung K. Chu |
| 205-217 | Polydeoxyaminohexopyranosylnucleosides. Synthesis of 1-(2,3,4-Trideoxy-3-nitro-β-D-erythro- and threo-hexopyranosyl)-uracils from Uridine | Akira Matsuda; Kyoichi A. Watanabe |
| 219-233 | Electrophilic Amination of Adenines. Formation and Characteristics of N-Aminoadenines | Tetsuya Saga; Toyo Kaiya; Shoji Asano; Kohfuku Kohda |
| 235-250 | Synthesis, Conformational Analysis, and Biological Activity of a Rigid Carbocyclic Analogue of 2′-Deoxy Aristeromycin Built on a Bicyclo[3.1.0]hexane Template | Maqbool A. Siddiqui; Harry Ford Jr.; Clifford George; Victor E. Marquez |
| 251-263 | Nucleosides and Nucleotides. 140. Synthesis and Antileukemic Activity of 5-Carbon-Substituted 1-β-d-Ribofuflranosylimidazole-4-Carboxamides | Noriaki Minakawa; Naoshi Kojima; Takuma Sasaki; Akira Matsuda |
| 265-286 | Synthesis, In Vitro Biological Stability, and Anti-HIV Activity of 5-Halo (or Methoxy)-6-Alkoxy (Azido or Hydroxy)-5,6-Dihydro-2′,3′-Didehydro-3′-Deoxythymidine Diastereomers as Potential Prodrugs of 2′,3′-Didehydro-3′-deoxythymidine (D4T) | Rakesh Kumar; Lili Wang; Leonard I. Wiebe; Edward E. Knaus |
| 287-304 | Synthesis and Biological Evaluation of 4′-C-Methyl Nucleosides | Toshiaki Waga; Hiroshi Ohrui; Hiroshi Meguro |
| 305-324 | Synthesis and Biological Evaluation of 1′-C-Cyano-Pyrimidine Nucleosides | Yuichi Yoshimura; Fumitaka Kano; Shuichi Miyazaki; Noriyuki Ashida; Shinji Sakata; Kazuhiro Haraguchi; Yoshiharu Itoh; Hiromichi Tanaka; Tadashi Miyasaka |
| 325-335 | Synthesis of 1,5-Anhydrohexitol Nucleosides as Mimics of AZT, D4T and DDC | Ilse Verheggen; Arthur Van Aerschot; Jef Rozenski; Gerard Janssen; Erik De Clercq; Piet Herdewijn |
| 337-347 | A Novel Type of Spironucleosides: 2′,5′-O-bis-TBDMS Uridine-3′-spiro-3′-isoxazolidin-5′-one and Its Thymidine Congener | Jean M. J. Tronchet; Imre Kovacs; Françoise Barbalat-Rey; Naz Dolatshahi |
| 349-359 | Novel Tsao Derivatives. Synthesis and Anti-HIV-1 Activity of Allofuranosyl-TSAO-T Analogues | Rosa Alvarez; Ana San-Félix; Erik De Clercq; Jan Balzarini; María José Camarasa |
| 361-378 | Nucleoside Phosphonates. Development of Synthetic Methods and Reagents | Annika Kers; Inger Kers; Adam Kraszewski; Michal Sobkowski; Tomas Szabó; Mats Thelin; Rula Zain; Jacek Stawinski |
| 379-386 | The 1,1-Dianisyl-2,2,2-trichloroethyl Moiety as a New Protective Group for the Synthesis of Dinucleostde Trifluoromethylphosphonates | Rosa Maria Karl; Wolfgang Richter; Roland Klösel; Michael Mayer; Ivar Ugi |
| 387-397 | Syntheses of 2′-O-Methylisocytidine Phosphoramidite and Methylphosphonamidite Synthons | Daguang Wang; Paul O. P. Ts'o |
| 399-406 | Isolation of Oligodeoxynucleoside Phosphorothioate Diastereomers by the Combination of DEAE Ion-Exchange and Reversed-Phase Chromatography | Hideyuki Kanehara; Masatsugu Mizuguchi; Keisuke Makino |
| 407-417 | Stereocontrolled Transesterification for the Synthesis of Chiral Phosphite Triester Backbone | Masatsugu Mizuguchi; Keisuke Makino |
| 419-430 | Purification of 5′-O-Trityl-on Oligoribonucleotides. Investigation of Phosphate Migration During Purification and Detritylation. | Bashar Mullah; Alex Andrus |
| 431-443 | Nucleosides, LVIII1 Synthesis of Base - Modified Oligonucleotides Containing 6- and 7-Aryl Lumazines | Yuris Maurinsh; Wolfgang Pfleiderer |
| 445-464 | Synthesis of 1-Deazaadenosine Analogues of (2′→5′) ApApA | Igor A. Mikhailopoulo; Elena N. Kalinichenko; Tatjana L. Podkopaeva; Thomas Wenzel; Helmut Rosemeyer; Frank L. Seela |
| 465-475 | Synthesis of Oligopeptides as Polynucleotide Analogs | Hiroki Umemiya; Hiroyuki Kagechika; Yuichi Hashimoto; Koichi Shudo |
| 477-488 | 19F NMR of RNA. The Structural and Chemical Aspects of 5-Fluoro-cytidine and-uridine Labelling of Oligoribonucleotides | Artur Fischer; Zofia Gdaniec; Ewa Biala; Marek Łożyński; Jan Milecki; Ryszard W. Adamiak |
| 489-503 | NMR Studies of a Lead Ribozyme and Its Non-Cleavable Analogue | Masato Katahira; Takashi Sugiyama; Mayumi Kanagawa; Mi Hee Kim; Seiichi Uesugi; Toshiyuki Kohno |
| 505-517 | Cleavage of Short RNAs Containing Higher Ordered Structures by Hammerhead Ribozymes | Makoto Koizumi; Tsutomu Ohta; Yasuo Komatsu; Eiko Ohtsuka |
| 519-529 | Properties and Anti-HIV Activity of Nicked Dumbbell Oligonucleotides | Hidefumi Yamakawa; Kazumi Hosono; Toshiaki Ishibashi; Hideki Nakashima; Takafumi Inagawa; Naoki Yamamoto; Kazuyuki Takai; Hiroshi Takaku |
| 1823-1829 | Interaction of RKRK Tetrapeptide with Polynucleotides | Ajay Kumar |
| 1831-1852 | Synthesis of 5′-Fluoro-5′-deoxy-and 5′-Amino-5′-Deoxytoyocamycin and Sangivamycin and Some Related Derivatives | Moheshwar Sharma; Yi X. Li; Miroslav Ledvina; Miroslav Bobek |
| 1853-1859 | Oligonucleotides Containing Acyclic Nucleoside Analogues with Carbamate Internucleoside Linkages | Ivan Habus; Sudhir Agrawal |
| 1861-1871 | Kinetic Properties of Adenine Nucleotide Analogues Against Purified 5-Phosphoribosyl-1-pyrophosphate Synthetases from E. coli, Rat Liver and Human Erythrocytes | J. Balzarini; J. F. Navé; M. A. Becker; M. Tatibana; E. De Clercq |
| 1873-1887 | Synthesis and Biochemical Activity of 5-Tethered Carborane-Containing Pyrimidine Nucleosides as Potential Agents for DNA Incorporation | Feng-Guang Rong; Albert H. Soloway; Seiichiro Ikeda; David H. Ives |
| 1889-1900 | A Simple Method for Synthesis of Spongosine, Azaspongosine, and Their Antiplatelet Effects | Lalit M. Ojha; Deepa Gulati; Neena Seth; Diwan S. Bhakuni; Ram Pratap; Kailash C. Agarwal |
| 1901-1904 | Synthesis of 2-Alkyl-3-hydroxy-4-pyridinone-ribonucleosides, Potential Oral Iron Chelators | Gang Liu; Fred W. Bruenger; Amy M. Barrios; Scott C. Miller |
| 1905-1912 | Synthesis of a Carboxamide Linked T*T Dimer with an Acyclic Nucleoside Unit and Its Incorporation in Oligodeoxynucleotides | Erik Larsen; Krzysztof Danel; Erik B. Pedersen |
| 1913-1927 | Fluorinated Carbaacyclonucleosides: Synthesis and Evaluation of Antiviral Activity | Maureen Lewis; T. Brian; H. McMurry; Erik De Clercq |
| 1929-1945 | Enantiospecific Synthesis of Carbocyclic Aminoimidazole Carboxamide Ribonucleotide (C-AICAR), Succinoaminoimidazole Carboxamide Ribonucleotide (C-SAICAR), and a New Intermediate for SAICAR Analogs | Laurent Schmitt; Carol A. Caperelli |
| 1947-1959 | Conformational Transitions in Poly d(CGCGCGTTAATT) | Ajay Kumar |
| 1961-1984 | Synthesis of 2′-Substituted Sulfide-Linked Dinucleotides | Daguang Wang; Bin; Masad J. Damha; George Just |
| 1985-1996 | Synthesis, Conformational and Configurational Studies of Some New Acetylated Glycosides of 2-Thio-3-aryl-4(3H)-quinazolinones, Their Thiono and 3,1-Benzothiazin-2,4-dithione | Mohamed F. Abdel-Megeed; Mohamed A. Saleh; Youssef L. Aly; Ibrahim M. Abdo |
| 1997-2008 | Synergistic Effect of 5-Nitro-2′-deoxyuridine with Ganciclovir Against Human Cytomegalovirus In Vitro | T. Sudhakar Rao; Robert F. Rando; John H. Huffman; Ganapathi R. Revankar |
| 2009-2025 | Building Blocks for Synthesis of Oligoarabinonucleotides: Preparation of Arabinonucleoside H-Phosphonates from Protected Ribonucleosides | Eriks Rozners; Erika Bizdena |
| 2027-2038 | Synthesis of a Carboxamide Linked UBr*UBr Dimer–Duplex and Triplex Stabilities of the Corresponding Oligodeoxynucleotides | Abdel Aleem H. Abdel Aleem; Erik Larsen; Erik B. Pedersen |
| 2039-2049 | A Short High Yielding Synthesis of the Potent Anti-VZV Carbocyclic Nucleoside Analogue Carba-BVDU | P. G. Wyatt; A. S. Anslow; B. A. Coomber; R. P. C. Cousins; D. N. Evans; V. S. Gilbert; D. C. Humber; I. L. Paternoster; S. L. Sollis; D. J. Tapolczay; G. G. Weingarten |
| 2051-2060 | The Synthesis and Biological Evaluation of Sulfamoyl Nucleosides Related to Carbovir and AZT | Robert Vince; Phuong T. Pham |
| 2061-2077 | Synthesis and Biological Activity of Cyclohexenyl Nucleosides. cis-5-(9H-Purin-9-yl)-3-cyclohexenyl Carbinols and Their 8-Azapurinyl Analogs | Michael J. Konkel; Robert Vince |
| 2079-2087 | Different Mechanisms of Inhibition of DNA Synthesis by (E)-5-(2-Bromovinyl)-2′-deoxyuridine in Cells Transfected with Gene for Thymidine Kinase of Herpes Simplex Virus Type 1 and in Cells Infected with the Virus | Yasuhide Hirota; Yujiro Arao; Akiko Matsumoto; Shiro Nii; Yusuke Wataya |
| 2089-2097 | Molecular Mechanism of 5-Fluoro-2′-deoxyuridine-induced dNTP Imbalance Cell Death: Purification of an Endonuclease Involved in DNA Double Strand Breaks During dNTP Imbalance Death | Hwa-shin Hwang; Masashi Ohtani; Tohru Nakazawa; Tatsushi Igaki; Osamu Masui; Shiro Kankawa; Chikao Nakayama; Sei Yoshida; Akiko Yoshioka-Hiramoto; Yusuke Wataya |
| 1465-1479 | Synthesis of Novel 3′-C-(Hydroxymethyl)thymidines and Oligodeoxynucleotide Analogues Containing Compressed 3′-C-Hydroxymethyl-Linked Phosphodiester Backbones | Jesper Wengel; Margit L. Svendsen; Pia N. Jørgensen; Claus Nielsen |
| 1481-1492 | Large Scale Synthesis of Oligoribonucleotides on High-Loaded Polystyrene (HLP) Support | Dean Tsou; Arnold Hampel; Alex Andrus; Ravi Vinayak |
| 1493-1502 | Synthesis of 3′,4′-C-Bishydroxymethyl-2′,3′,4′-trideoxy-β-L-threo-pentopyranosyl Nucleosides as Potential Inhibitors of HIV | Åsa Lundquist; Ingemar Kvarnström; Stefan C. T. Svensson; Björn Classon; Bertil Samuelsson |
| 1503-1518 | Interaction of (2′ -5′) and (3′ -5′) Linked 2-Aminoadenylyl-3-aminoadenosines with Polyuridylic Acid | Masako Muraoka; Seizo Takahashi; Seiichi Uesugi |
| 1519-1537 | Isolation and Characterization of an Unusual Nucleoside, 1-α-D-Ribofuranosyl-4-pyridone-3-carboxamide, from the Urines of Normal Human Individuals and Leukemic Patients | G. B. Chheda; H. B. Patrzyc; H. A. Tworek; S. P. Dutta |
| 1539-1543 | A New Synthesis of 2′,3′-Didehydro-3′-deoxy-3-Alkylthymidine | G. Negrón; B. Quiclet-Sire; Y. Diaz; R. Gaviño; R. Cruz |
| 1545-1558 | Synthesis, Bioactivation and Anti-HIV Activity of 4-Acyloxybenzyl bis(Nucleosid-5′-yl) Phosphates | Anne Routledge; Ian Walker; Sally Freeman; Alan Hay; Naheed Mahmood |
| 1559-1579 | Evaluation of the Kinetics of Hydrolysis of Monoamino Analogues of 2′- or 3′-Deoxyadenosine and of 9-(2-Deoxy-β-D-Threo-pentofuranosyl)Adenine or 9-(3-Deoxy-β-D-threo-pentofuranosyl)Adenine by Liquid Chromatography | Grace Thoithi; Ann Van Schepdael; Roger Busson; Piet Herdewijn; Eugène Roets; Jos Hoogmartens |
| 1581-1590 | Synthesis and Antiviral Activity of Some N-Pentopyranosyl-2-Pyridinethiones | Adel M. E. M. Attia; Elsayed I. Ibrahim; Fouad E. A. Hay; Mohammed M. A. Abbasi; Hanaa A. E. Mansour |
| 1591-1600 | An Efficient Synthesis of 2-[(4-Amino∼1,2-dihyro-2-oxo-1- pyrimidinyl)methoxyi-l,3-propanediyl-di-L-valinate an Anti-cytomegalovirus Agent | Nabih Ghal; Barbara Johnston; Lilia Beauchamp; Taj Naseree; Tracy Scott; Roy Flanagan; Martha Rodriguez |
| 1601-1612 | Synthesis of Certain Acyclic Nucleoside Analogs of 1,2,4-Triazolo[3,4-f][1,2,4]triazine and Pyrimido[5,4-d]pyrimidine | T. Sudhakar Rao; Ganapathi R. Revankar |
| 1613-1617 | Note: A Convenient Method for the Preparation of N2, N2-Dimethylguanosine | Anna Maria Aviñó; Adrian Mayordomo; Ruth Espuny; Montse Bach; Ramon Eritja |
| 1163-1177 | Preparation and 17O NMR Spectra of 17O-Labeled Thymidine 5′-Phosphate Triesters, Alkylphosphonates, Dialkylphosphinates, and Phosphoramidates | T. Sudhakar Rao; A. E. Sopchik; Wesley G. Bentrude |
| 1179-1193 | Conformational Studies on Deoxyribonucleosides of C6-Substituted Pyrimidines | Shashidhar N. Rao |
| 1195-1210 | Oligodeoxynucleotides Embodying the Ambiguous Base Z, 5-Amino-imidazole-4-carboxamide | Sylvie Pochet; Laurence Dugué |
| 1211-1218 | Nucleic Acid Related Compounds: A Convenient Synthesis of 3-Deazauridine Analogues | Adel M. E. Attia; Galal E. H. Elgemeie |
| 1219-1226 | Large-Scale Synthesis of Oligodeoxyribonucleotide Phosphorothioate Using Controlled-Pore Glass as Support | Vasulinga T. Ravikumar; Mark Andrade; Tadeusz K. Wyrzykiewicz; Anthony Scozzari; Douglas L. Cole |
| 1227-1232 | Efficient Transformation of Thymidine into 2′,3′-Didehydro-2′,3′-Dideoxy-Thymidine (D4T) Involving Opening of a 2,3′-Anhydro Derivative by Phenylselenol | Stéfan Becouarn; Stanislas Czernecki; Jean-Marc Valéry |
| 1233-1249 | Synthesis and Antiviral Activity of Carbocyclic 5-Substituted Uridines and Cytidines | Anne Popescu; Anna-Britta Hörnfeldt; Salo Gronowitz |
| 1251-1258 | The X-ray Crystal and Molecular Structure of 5-Amino-1-(2,3:5,6-Di-O-isopropylidene-α-D-mannofuranosyl) Imidazole-4-carboxamide | C. E. Briant; D. W. Jones; G. Shaw |
| 1259-1267 | Solid Phase Synthesis of 2′, 5′-Oligoadenylates Containing 3′-Fluorinated Ribose | Teréz Kovács; Arthur Van Aerschot; Piet Herdewijn; Paul F. Torrence |
| 1269-1287 | A Practical Synthesis of N1-Methyl-2′-deoxy-ψ-uridine (ψ-Thymidine) and Its Incorporation into G-Rich Triple Helix Forming Oligonucleotides | Birendra K. Bhattacharya; Rodrigo V. Devivar; Ganapathi R. Revankar |
| 1289-1300 | Synthesis, Conformation of 3′-(Tetrazole-2″-yl)-3′-deoxythymidine and its 5″-Derivatives. Substrate Properties of 3′-(Tetrazole-2″-yl)-3′-deoxythymidine 5′-Triphosphate | V. A. Ostrovskii; E. P. Studentsov; V. S. Poplavskii; N. V. Ivanova; G. V. Gurskaya; V. E. Zavodnik; M. V. Jasko; D. G. Semizarov; A. A. Krayevsky |
| 1301-1314 | Structural Characterization of Cyclic ADP-Ribose by NMR Spectroscopy | Takeshi Wada; Kiyoshi Inageda; Keiichi Aritomo; Ken-ichi Tokita; Hiroshi Nishina; Katsunobu Takahashi; Toshiaki Katada; Mitsuo Sekine |
| 1315-1327 | Synthesis and Antiviral (RNA) Evaluation of Nucleoside Analogs of Tiazofurin Modified at the Carboxamide Moiety | Michael J. Phelan; Bjarne Gabrielsen; Jorma J. Kirsi; William M. Shannon; Michael A. Ussery; Louis Barthel-Rosa; Ernst M. Schubert; Ganesh D. Kini; Roland K. Robins |
| 1329-1339 | Efficient Synthesis of 2′-Amino-2′-deoxypyrimidine 5′-Triphosphates | Danny P. C. McGee; Chandra Vargeese; Yansheng Zhai; Gary P. Kirschenheuter; Alecia Settle; Colleen R. Siedem; Wolfgang A. Pieken |
| 1341-1348 | Synthesis and Reactions of Some Glycosylamine Derivatives of 6-Azauracil Nucleosides | Najim A. Al-Masoudi; Ali A. Al-Atoom |
| 1349-1357 | Improved Procedure for the Reduction of N - 1 Content in Synthetic Oligonucleotides | Radhakrishnan P. Iyer; Dong Yu; Zhiwei Jiang; Sudhir Agrawal |
| 1359-1377 | Solid State and Solution Structure and Conformation of The Antiviral Acyclonucleoside 9-[4-Hydroxy-2-(hydroxymethyl)-butyl]guanine | Karin Bjåmer Birnbaum; Ryszard Stolarski; David Shugar |
| 1379-1392 | Synthesis of New Thiazolidinone Nucleoside Analogues | J. C. Graciet; P. Faury; M. Camplo; A. S. Charvet; N. Mourier; C. Trabaud; V. Niddam; V. Simon; J. L. Kraus |
| 1393-1402 | Peptide-Nucleoside Conjugates: Synthesis and Anti-HIV Activities | Nicolas Mourier; Carole Trabaud; Jean Christophe Graciet; Vanessa Simon; Valérie Niddam; Philippe Faury; Anne Sophie Charvet; Michel Camplo; Jean-Claude Chermann; Jean Louis Kraus |
| xxiii-xxiv | Preface | E. De Clercq |
| 279-282 | Synthesis of 3′-4′-α-Propylene-2′-3′-dideoxynucleosides | Magnus Björsne; Tomas Szabó; Bertil Samuelsson; Björn Classon |
| 283-286 | Synthesis and Anti-viral Properties of 2′,3′-Dideoxy-3′,4′-dihydroxymethyl Substituted Pyrimidine Nucleoside Analogues | Magnus Björsne; Björn Classon; Inger Kers; Bertil Samuelsson; Ingemar Kvarnström |
| 287-290 | Tautomerism and Regioselectivity in Ribosylation of Guanine | Jerzy Boryski; Andrzej Manikowski |
| 291-293 | The Synthesis of Bicyclic N4-Amino-2′-deoxycytidine Derivatives | D. Loakes; D. M. Brown |
| 295-297 | Carbocyclic Nucleosides with a Modified Cyclopentane Skeleton | O. Caamaño; F. Fernández; G. Gómez; M. I. Nieto |
| 299-301 | Synthesis of [1-[2′,5′-bis-O-(t-Butyldimethylsilyl)-β- L-ribofuranosyl] thymine]-3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″,2″-dioxide) (L-TSAO-T) | Simon Ingate; Ana San-Félix; Erik De Clercq; Jan Balzarini; Maríia-José Camarasa |
| 303-305 | Asymmetric Synthesis of Cyclopropyl Carbocyclic Nucleosides | Y. F. Zhao; M. G. Lee; T. -F. Yang; B. K. Chun; J. F. Du; R. F. Schinazi; C. K. Chu |
| 307-309 | Radical Mediated Synthesis of 3′-α-C-Allenyl-2′,3′-dideoxythymidine as a Non-polar Analogue of AZT | S. Becouarn; S. Czernecki; J. M. Valéry |
| 311-312 | Simple Synthesis of the 5-O-Benzoylriboside of 1,4-Dihydronicotinic Acid; a Cofactor for DT Diaphorase and Nitroreductase Enzymes | Lawrence C. Davies |
| 313-316 | Novel Analogues of Tiazofurin by Lawesson Reagent Effected Cyclization | Bozenna Golankiewicz; Piotr Januszczyk |
| 317-320 | Synthesis of the β-2′,3′-Unsaturated Pentopyranosyl Nucleosides and Their 3′-Hydroxymethyl Congeners | Bogdan Doboszewski; Norbert Blaton; Piet Herdewijn |
| 321-324 | Synthesis of 1,5-Anhydro-2-(N6-Cyclopentyladenin-9-Yl)-2-Deoxy-D-Altrohexitol | I. Verheggen; A. Van Aerschot; N. Pillet; E. M. van der Wenden; A. Ijzerman; P. Herdewijn |
| 325-328 | Synthetic Approaches to 5:8-Fused Heterocyclic Systems. A Novel Rearrangement During the Synthesis of Imidazo[4,5-e][1,2,4]triazocine Ring System | Friedrich N. Burnett; Ramachandra S. Hosmane |
| 329-332 | Synthesis of Analogues of 3′-Deoxypsicothymidine | Jari Hovinen; Alex Azhayev; Andrei Guzaev; Harri Lönnberg |
| 333-336 | Highly Diastereoselective Synthesis of (2′S)-[2′-2H]-2′-Deoxyribonucleosides from the Corresponding Ribonucleosides | Etsuko Kawashima; Yukio Aoyama; Mohamed F. Radwan; Masayoshi Miyahara; Takeshi Sekine; Masatsune Kainosho; Yoshimasa Kyogoku; Yoshiharu Ishido |
| 337-340 | Synthesis of 9-(2-Hydroxyethoxymethyl)guanine (Acyclovir) from Guanosine | Hiroshi Shiragami; Yoshihito Koguchi; Yasuhiro Tanaka; Satoshi Takamatsu; Yumiko Uchida; Takashi Ineyama; Kunisuke Izawa |
| 341-344 | Synthesis of “Reversed” and “Double Headed” Nucleosides | B. Kašnar |
| 345-347 | Synthesis of 3′-C-Phosphono Nucleosides from α,β-Unsaturated Lactone | Thomas Kofoed; Erik B. Pedersen |
| 349-352 | Synthesis of Fluorescent Adenosine Analogues1 | R. F. de Boer; D. G. I. Petra; M. J. Wanner; A. Boesaart; G. J. Koomen |
| 353-356 | Synthesis of Acycloalkenyl Derivatives of Pyrimidines and Purines | H. B. Lazrek; N. Redwane; A. Rochdi; J. L. Barascut; J. -L. Imbach; E. De Clercq |
| 357-358 | Carbocyclic Nucleosides: Synthesis of Analogues of Cyclobut-G | F. Fernández; M. C. López; A. R. Hergueta |
| 359-362 | Synthesis of 2-Deoxy-4-thio-D-ribofuranose and Its 3-Azido Analogue from L-Arabinose; Intermediates in the Synthesis of 4′-Thiodeoxynucleosides | H. Ait sir; D. F. Ewing; N. Fahmi; G. Goethals; G. Mackenzie; G. Ronco; B. Tber; P. Villa |
| 363-366 | The Synthesis of Novel Transition State Analogues Related to Imidazole and Purine Nucleotides Involved in the De novo Biosynthesis of Purines | A. Scott Frame; Richard H. Wightman; G. Mackenzie |
| 367-368 | A Regiospecific and Stereoselective Rearrangement of a 1-β-D-Ribofuranosyl-5-aminoimidazole to a 4-β-D-Ribofuranosylaminoimidazole | David F. Ewing; Graharne Mackenzie; Sean P. N. Rouse; Richard M. Scrowston |
| 369-372 | A Novel Synthesis of Mizoribine® and Related Nucleosides from Acyclic Precursors | David F. Ewing; Robert W. Humble; Grahame Mackenzie; Gordon Shaw |
| 373-375 | Acyclic Nucleoside and Nucleotide Analogues with Amide Bond | E. V. Efimtseva; S. N. Mikhailov; M. V. Jasko; D. V. Malakhov; D. G. Semizarcv; M. V. Fomicheva; E. R. Kern |
| 377-380 | Synthesis of Sugar Modified Nucleosides Containing Nicotinic, Quinaldic, Indol-3-ylpropionic or 1-Nitroanthraquinone-2-carboxylic Acid Residue | S. Ya. Melnik; L. V. Ektova; O. V. Goryunova; E. V. Khorysheva; S. V. Makutova; I. L. Plikhtyak; I. V. Yartseva |
| 381-382 | Epimerization at C2 of Methyl 5-O-Benzyl-2-deoxy-2-fluoro-α-D-pentofuranosides upon Oxidation | Igor A. Mikhailopulo; Grigorii G. Sivets; Nicolai E. Poopeiko; Natalia B. Khripach |
| 529-532 | Synthesis and Biological Activities of Sugar-Modified 2-(p-n-Butylanilino)-2′-deoxyadenosine Analogues | Toyofumi Yamaguchi; Kunie Sato; Mineo Saneyoshi |
| 533-536 | Stereospecific Synthesis and Anti-HIV Activity of (Z)2′- and (E)3′-Deoxy-2′(3′)-C-(chloromethylene) Pyrimidine Nucleosides | Elena N. Kalinichenko; Elena B. Rubinova; Evgueny V. Borisov; Jan Balzarini; Erik De Clercq; Igor A. Mikhailopulo |
| 537-539 | Strategically Functionalized Adenosines: Agonists for Adenosine Receptors | Vasu Nair; Steven A. Adah; Seung B. Ha |
| 541-544 | Synthesis and Antiviral Evaluation of 3′-Substituted Thymidine Analogues Derived from 3′-Amino-3′-deoxythymidine | C. Pannecouque; K. Van Poppel; J. Balzarini; P. Claes; E. De Clercq; P. Herdewijn |
| 545-547 | The Synthesis and Antiviral Activity of Some New S-Adenosyl-L-homocysteine Derivatives and Their Nucleoside Precursors | Pawel Serafinowski; Erwin Dorland; Jan Balzarini; Erik De Clercq |
| 549-550 | Synthesis and Antiviral Evaluation of 3′-Deoxy-β-L-erythro-pentofuranosyl Nucleosides of the Five Naturally Occurring Nucleic Acid Bases | C. Mathé; G. Gosselin; M. -C. Bergogne; A. -M. Aubertin; G. Obert; A. Kirn; J. -L. Imbach |
| 551-554 | Synthesis and Antiviral Activity of 2 and 3-Substituted Imidazo[1,2-a]pyrimidine | A. Gueiffier; Y. Blache; J. P. Chapat; A. Elhakmaoui; E. M. Essassi; G. Andrei; R. Snoeck; E. De Clercq; O. Chavignon; J. C. Teulade; F. Fauvelle |
| 555-558 | Synthesis and Biological Activity of Sugar-Fluorinated 2′,3′-dideoxy-4′-thioribofuranosyl Nucleosides | Victor E. Marquez; Lak S. Jeong; Marc C. Nicklaus; Cliff George |
| 559-562 | Combination of Azidothymidine (AZT) and (E)-5-(2-Bromovinyl)-2′-deoxyuridine (BVDU) Inhibits the Replication of Herpes Simplex Virus Type 1 (HSV-1) and Type 2 (HSV-2) and Varicella Zoster Virus (VZV) Strains That Are Deficient in the Expression of the Viral Thymidine Kinase (tk) | G. Andrei; R. Snoeck; J. Balzarini; E. De Clercq |
| 563-565 | New Prodrugs of 9-(2-Phosphonomethoxyethyl)adenine [PMEA]: Synthesis and Stability Studies | S. Benzaria; G. Gosselin; H. Pelicano; G. Maury; A. -M. Aubertin; G. Obert; A. Kirn; J. -L. Imbach |
| 567-570 | Antiviral Activity of Selected Nucleoside Analogues Against Human Herpes Virus Type 6 | D. Reymen; L. Naesens; J. Balzarini; A. Holy; E. De Clercq |
| 571-574 | Anti-herpes Activities of Isonucleoside Analogues with Variable Bases at the 2′ Position | T. Kira; A. Kakefuda; S. Shuto; A. Matsuda; M. Baba; S. Shigeta |
| 575-583 | Hept Derivatives: 6-Benzyl-1-ethoxymethyl-5-isopropyluracil (MKC-442) | Masanori Baba; Hlromichi Tanaka; Tadashi Miyasaka; Satoshi Yuasa; Masaru Ubasawa; Richard T. Walker; Erik De Clercq |
| 585-594 | TSAO Derivatives: Highly Specific Inhibitors of Human Immunodeficiency Virus Type-1 (HIV-1) Replication | Maria J. Camarasa; Maria J. Péarez-Péarez; Sonsoles Velázquez; Ana San-Féalix; Rosa Alvarez; Simon Ingate; Maria Luisa Jimeno; Anna Karlsson; Erik De Clercq; Jan Balzarini |
| 595-598 | Synthesis and Anti-HIV-1 Activity of 4- and 5-Substituted 1,2,3-Triazole-TSAO Derivatives | Ana San-Féalix; Rosa Alvarez; Sonsoles Veláazquez; Erik De Clercq; Jan Balzarini; María José Camarasa |
| 599-602 | Evidence for the Involvement of the Small Subunit of HIV-1 Reverse Transcriptase (RT) in the TSAO-Resistance | Heidi Jonckheere; Jean-Marc Taymans; Jan Balzarini; Sonsoles Veláazquez; Maria Jose Camarasa; Jan Desmyter; Erik De Clercq; Jozef Annéa |
| 603-606 | Inhibitory Effects of 1-Deazaadenosine Analogues on HIV Replication and Adenosine Deaminase | Sauro Vittori; Rosaria Volpini; Emidio Camaioni; Giorgio Palúg; Giorgio Cristalli |
| 607-610 | Acyclic Nucleotides Related to Clitocine: Synthesis and Anti-HIV Activity | P. Franchetti; L. Cappellacci; G. Abu Sheikha; M. Grifantini; A. G. Loi; A. De Montis; M. G. Spiga; P. La Colla |
| 611-617 | 2′-and/or 3Y-Deoxy-β-L-pentofuranosyl Nucleoside Derivatives: Stereospecific Synthesis and Antiviral Activities | Gilles Gosselin; Christophe Mathé; Marie-Christine Bergogne; Anne-Marie Aubertin; Andre Kirn; Jean-Pierre Sommadossi; Raymond Schinazi; Jean-Louis Imbach |
| 619-625 | Studies of the Pharmacokinetics and Toxicology of 2′,3′-Dideoxy-β-L-5-fluorocytidine (β-L-FddC) and 2′,3′-Dideoxy-β-L-cytidine (β-L-ddC) In Vivo; and Synthesis and Antiviral Evaluations of 2′,3′-Dideoxy-β-L-5-azacytidine | Tai-Shun Lin; Xin Guo; Mei-Zhen Luo; Mao-Chin Liu; Yong-Lian Zhu; Ginger E. Dutschman; S. Balakrishna Pai; Mao-Mi Li; Yung-Chi Cheng |
| 627-635 | Structure-Activity Relationships Among a New Class of Antiviral Heterosubstituted 2′,3′-Dideoxynucleoside Analogues | Tarek S. Mansour; Haolun Jin; Wei Wang; Dilip M. Dixit; Colleen A. Evans; H. L. Allan Tse; Bernard Belleau; John W. Gillard; Elizabeth Hooker; Claire Ashman; Nick Cammack; Horacio Salomon; Antonietta R. Belmonte; Mark A. Wainberg |
| 637-640 | Synthesis, Antitumor Activity and Crystallographic Studies of Analogues of Tiazofurin | L. Cappellacci; P. Franchetti; M. Grifantini; L. Messini; G. Abu Sheikha; G. Nocentini; R. Moraca; B. M. Goldstein |
| 641-644 | Modulators of Nucleotide Metabolism Inhibit HIV Replication in Lymphoid Cells and Affect Its Inhibition by Dideoxynucleosides | Ranga V. Srinivas; Yi-Fei Gong; Anna Becher; Arnold Fridland |
| 645-647 | Synthesis and Antitumor Properties of Some Neutral Triesters of 5-Fluoro-2′-deoxyuridine-5′-monophosphate and 3′,5′-Cyclic Monophosphate | J. -L. Girardet; G. Gosselin; C. Périgaud; J. Balzarini; E. De Clercq; J. -L. Imbach |
| 649-652 | Induction of Erythroid Differentiation of Human Leukemia K562 Cells by the Acyclic Nucleoside Phosphonate 9-(2-Phosphonylmethoxyethyl)adenine (PMEA) | S. Hatse; J. Balzarini; E. De Clercq |
| 653-656 | Synthesis and Antitumour Properties of 2-Thio-5-chloro-nucleosides | K. Felczak; M. Bretner; M. Balińska; J. M. Dzik; W. Rode; T. Kulikowski |
| 657-660 | Synthesis and Biological Activity of 5-Fluoro-2-thiocytosine Nucleosides | M. Bretner; M. Balinska; K. Krawiec; B. Kierdaszuk; D. Shugar; T. Kulikowski |
| 661-664 | Three-Dimensional Cell Cultures as a Model System to Evaluate the Biological Activity of Gemcitabine (2′, 2′-Difluoro-2′deoxycytidine) | Godefridus J. Peters; Evelien Smitskamp-Wilms; Gijsbert Veerman; Paulo E. Pizao; Veronique W. T. Ruiz van Haperen; Herbert M. Pinedo |
| 665-669 | Studies on 6-Mercaptopurine Cytotoxicity in Molt F4 Human Malignant T-Lymphoblasts | E. H. Stet; R. A. De Abreu; J. P. M. Böukkerink; J. M. F. Trijbels |
| 671-674 | Synthesis and Broad-Spectrum Antiviral Activity in Mice of Certain Alkyl, Alkenyl and Ribofuranosyl Derivatives of 7-Deazaguanine | G. R. Revankar; T. S. Rao; K. Ramasamy; D. F. Smee |
| 675-686 | The Synthesis and Biological Activity of Certain 4′-Thionucleosides | John A. Secrist III; William B. Parker; Kamal N. Tiwari; Lea Messini; Sue C. Shaddix; Lucy M. Rose; L. Lee Bennett Jr; John A. Montgomery |
| 689-692 | An Improved Synthesis of N6-(6-Aminohexyl)FAD | Ashty Saleh; Frans Compernolle; Gerard Janssen |
| 693-694 | A Convenient Method for the Synthesis of ATP and Ap4A | Koichiro Fukuoka; Fuminori Suda; Masahide Ishikawa; Tsujiaki Hata |
| 695-702 | Acyclic Nucleotide Analogues and Related Compounds | Antonín Holý; Hana Dvořáková |
| 703-706 | Studies on Aryl H-Phosphonates. Synthesis of Nucleoside N-Alkylphosphonamidates | Anna Sobkowska; Michał Sobkowski; Jacek Stawiski; Adam Kraszewski |
| 707-710 | Phosphonates Derivatives of 2′,3′-Dideoxy-2′,3′-didehydro-pentopyranosyl Nucleosides | María-Jesús Péarez-Péarez; Bogdan Doboszewski; Erik De Clercq; P. Herdewijn |
| 711-714 | Conversion of Nucleoside H-Phosphonate Monoesters to the Corresponding H-Phosphonothioates. 31P NMR Studies | Jacek Stawiński; Rula Zain |
| 715-716 | 2-Cyanoethyl H-Phosphonate. A Reagent for the Mild Preparation of Nucleoside H-Phosphonate Monoesters | Tomas Szabóa; Helena Almer; Roger Ströumberg; Jacek Stawinski |
| 717-721 | Synthesis and Properties of P1, P2-, P1, P3- and P1, P4-Dinucleoside Di-, Tri- and Tetraphosphate mRNA 5′-Cap Analogues | J. Steogon; piński; M. Bretner; M. Jankowska; K. Felczak; R. Stolarski; Z. Wieczorek; A-L. Caipostalcode; R. E. Rhoads; A. Temeriusz; D. Haber; E. Darzynkiewicz |
| 723-726 | Synthesis of Four Stereoisomers of Carbocyclic 5′-NOR D4A and Evaluation of Their Triphosphates as Substrates for DNA Polymerases | Natalia Dyatkina; Dniitry Semizarov; Lyubov Victorova; Alexander Krayevsky; Fritz Theil; Martin von Janta-Lipinski |
| 727-729 | Synthesis of Dioxolane Analogues of Dideoxynucleotides and Their Substrate Properties in DNA Synthesis Reactions | E. V. Efimtseva; S. N. Mikhailov; L. S. Victorova; T. A. Rosovskaya; R. Sh. Beabealashvilli |
| 731-734 | Methylene and Halomethylene Analogues of Diadenosine 5′,5″-P1, P3-Triphosphate (ApppA) as Substrates or Inhibitors of ApppA-Degrading Enzymes | Andrzej Guranowski; Elżibieta Starzyńska; Lidia Gzik; Steve P. Langston; Paul Brown; G. Michael Blackburn |
| 735-738 | Does Interaction of dNTP Glycone with an Active Center of Reverse Transcriptases Takes Place? A Model for a Binding Site | Alexander A. Krayevsky; Natalya B. Dyatkina; Marina K. Kukhanova |
| 739-742 | Qualitative and Quantitative Analysis of Cyclic Nucleotides and Related Enzymes by Static and Dynamic Fast Atom Bombardment Mass Spectrometry | James I. Langridge; A. Gareth Brenton; Terry J. Walton; Frank M. Harris; Russell P. Newton |
| 743-747 | Cytidine 3′,5′-Cyclic Monophosphate: A Third Cyclic Nucleotide Secondary Messenger? | Russell P. Newton |
| 749-751 | Novel Open-Chain Nucleotides Imitating 2′,3′-Dideoxy-2′,3′-Didehydronucleotides: Synthesis and Substrate Properties Toward DNA Polymerases | E. A. Shirokova; N. B. Tarussova; A. V. Shipitsin; D. G. Semizarov; M. Hieber; A. A. Krayevsky |
| 753-757 | Investigation of a Proposed Mechanism for Genotoxic Effects Induced by 2-Hydroxyalkylating Agents. Kinetics of Intramolecular Transesterification in Dithymidine 2-Hydroxyethyl-and 2-Hydroxypropyl Phosphate | E. Pettersson; E. Bergmark; U. Rannug; L. Ehrenberg; R. Ströumberg |
| 759-762 | Homo Dinucleoside-α-hydroxyphosphonate Diesters as Prodrugs of the Antiviral Nucleoside Analogues 2′,3′-Dideoxythymidine and 3′-Azido-2′,3′-dideoxythymidine | Chris Meier; Lothar Habel; Wolfgang Laux; Erik De Clercq; Jan Balzarini |
| 763-766 | Synthesis, Decomposition Pathways and “In Vitro” Evaluation of Bioreversible Phosphotriesters of Azt | Isabelle Lefebvre; Alain Pompon; Christian Périgaud; Jean-Luc Girardet; Gilles Gosselin; Anné-Marie Aubertin; Andre Kirn; Jean-Louis Imbach |
| 767-770 | In vivo Antiretroviral Efficacy of Oral bis(POM)-PMEA, the bis(Pivaloyloxymethyl)prodrug of 9-(2-Phosphonylmethoxyethyl) adenine (PMEA) | L. Naesens; J. Neyts; J. Balzarini; N. Bischofberger; E. De Clercq |
| 771-775 | Synthesis and Properties of mRNA 5′-Cap Analogues with 7-Methylguanine Replaced by Benzimidazole or 3-Methylbenzimidazole | L. Chlebicka; Z. Wieczorek; R. Stolarski; J. Stepinski; E. Darzynkiewicz; D. Shugar |
| 777-781 | Biological Activity of Some Dialkyl α-Anilinobenzylphosphonates and Their Palladium(II) Complexes | Lj. Tušek-Božić; M. Ćurić; J. Balzarini; E. De Clercq |
| 783-787 | Synthesis of Nucleotide Lipophilic Prodrugs Containing Two Inhibitors Targeted Against Different Phases of the HIV Replication Cycle | D. Bonnaffé; B. Dupraz; J. Ughetto-Monfrin; A. Namane; T. Huynh Dinh |
| 789-791 | bis(S-Acyl-2-thioethyl)esters of 2′,3′-Dideoxyadenosine 5′-Monophosphate Are Potent Anti-HIV Agents in Cell Culture | C. Périgaud; G. Gosselin; S. Benzaria; J. -L. Girardet; G. Maury; H. Pélicano; A. -M. Aubertin; A. Kirn; J. -L. Imbach |
| 795-798 | Synthesis of Base-Modified Oligonucleotides Containing 6- and 7-Aryl Lumazines | Yuris Maurinsh; Wolfgang Pfleiderer |
| 799-801 | Synthesis of 2′-C-Difluoromethyl Substituted Nucleoside Analogs as Ribonucleoside Replacements in Hammerhead Ribozymes | Martin Dunkel; Vivian Reither; Susanne Ebel-Will; János Ludwig |
| 803-804 | Synthesis of Protected 3′,5′-Di-2′-Deoxythymidine-(α-hydroxy-2-nitrobenzyl)-phosphonate Diesters as Dimer Building Blocks for Oligonucleotides | Chris Meier; Ralf Mauritz |
| 805-808 | Chemical and Enzymatic Synthesis of 2′-Deoxy-iso-inosine and Its Incorporation into DNA | Jean-Jacques Beaussire; Sylvie Pochet |
| 809-812 | The Application of H-Phosphonate Chemistry in the HELP Synthesis of Oligonucleotides | S. Zaramella; G. M. Bonora |
| 813-816 | Peptide Analogues of DNA Consisting of l-α-Amino-γ-thymine Butyric Acid and l-Valine Subunits | G. Ceulemans; K. Khan; A. Van Schepdael; P. Herdewijn |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 14, Number 1-2 | |
| 1-12 | Incorporation of 2′-Deoxy-9-deazaguanosine and 2′-Deoxy-7-deaza-6-thioguanosine into G-Rich Oligodeoxyribonucleotides | T. Sudhakar Rao; Arthur F. Lewis; Theresa Schmaltz Hill; Ganapathi R. Revankar |
| 13-22 | Characterization of Nucleoside Phosphotransferase from Leishmania Tropica | Il-Shik Shin; Yusuke Wataya |
| 23-37 | Synthesis, Molecular and Crystal Structure of 3′-N-Alkylamino-3′-deoxythymidines and Some Biochemical Properties of Their Phosphorous Esters | Maxim V. Jasko; lvati I. Fedorov; Alexey M. Atrazhev; Diriiitry Yu. Mozzherin; Nicolay A. Novicov; Alexey V. Bochkarev; Gnliiia V. Gurskaya; Alexander A. Krayevsky |
| 39-44 | 6-Deoxycarbovir: A Xanthine Oxidase Activated Prodrug of Carbovir | Robert Vince; Jay Brownell; Scott A. Beers |
| 45-63 | An Improved Synthesis of 1-(2-Deoxy-β-D-erythro-pentofuranosyl)quinazoline-2,4(3H)-dione and Its Incorporation Into G-Rich Triple Helix Forming Oligonucleotides | Birendra K. Bhattacharya; Mohan V. Chari; Ross H. Durland; Ganapathi R. Revankar |
| 65-76 | Synthesis of 2-Azido-1,N6-Etheno and 2-Azido Analogs of Deoxyadenosine as Nucleotide Photoaffinity Probes | Diane Flaherty; Preeti Balse; Ke Li; Bob M. Moore; Michael B. Doughty |
| 77-89 | Transglycosylation of β-D-RIbofuranosylindazoles | Jerzy Boryski |
| 91-103 | Synthesis and Substrate Properties of Thymidine 5′-Triphosphate Analogs with Large Hydrophobic Substituent Groups At α-P Atom | N. Dyatkina; A. Arzumanov; L. Victorova; M. Kukhanova; A. Krayevsky |
| 105-116 | Palladium-Mediated Coupling Reactions of an Aminosubstituted Heterocycle. Direct Synthesis of C-Nucleosides Related to Adenosine | Han-Cheng Zhang; Mohamed Brakta; G. Doyle Daves Jr. |
| 117-127 | Synthesis of an Uncharged cAMP-Analogue | G. Ceulemans; F. Vandendriessche; J. Rozenski; P. Herdewijn |
| 129-142 | Synthesis of 6-Substituted Purine N7-(2-Deoxy-β-D-Ribonucleosides) via Anion Glycosylation and Anomerization During the N7/N9-Glycosyl Transfer | Frank Seela; Holger Winter |
| 143-165 | RNA Modified Uridines VII: Chemical Synthesis and Initial Analysis of tRNA D-Loop Oligomers with Tandem Modified Uridines | Barbara Nawrot; Andrzej Malkiewicz; Wanda S. Smith; Hanna Sierzputowska-Gracz; Paul F. Agris |
| 167-173 | A Convenient and Efficient Method for the Synthesis of Nucleoside H-Phosphonates Using a Novel Phosphonylating Agent | Zai-Wan Yang; Zu-Sheng Xu; Nan-Zhen Shen; Zhi-Qiang Fang |
| 175-183 | The Evaluation OF 2′, 3′-Dideoxy-β-D-Erythro-Hex-2′-Enopyranosyl Nucleosides as Potential Antisense Constructs: Synthesis, Biophysical Properties and Enzymatic Stability of 2′-Deoxyadenosine-(3′–6′)-[1-(2′, 3′-Dideoxy-β-D-Erythro-Hex-2′-Enopyranosyl)thymine] Phosphate | Leslie W. Tari; Krishan L. Sadana; Anthony S. Secco |
| 185-194 | 3′-C-Trifluoromethyl Ribonucleosides | Carl R. Johnson; Dilip R. Bhumralkar; Erik De Clercq |
| 195-207 | Synthesis of (±)-cis-1-[2-(Hydroxymethyl)-1, 3-Oxathiolan-5-yl]cytosine and Its (±)-trans Isomer | Jim J. Huang; Janet L. Rideout; Gary E. Martin |
| 209-218 | Synthesis of Pyrimidine 2′,3′-Dideoxy-2-Thionucleosides | Bhalchandra V. Joshi; Colin B. Reese; Chamakura V. N. S. Varaprasad |
| 219-228 | Introduction of an Immunochemical Label in a Cytidine Analogue | Chryslaine R. Tanty; Lilia López-Canovas; Adamari López Brauet; Marelys Rivero Paredes; David Higginson Clarke; Herman Vélez Castro; Ana Ma. Riverón Rojas; Arturo Macías Cabrera |
| 229-241 | Oligonucleotides and Nucleotide-Peptides. LV. Synthesis and Some Properties of Triesters of Hydroxy Aming Acids and Thymidilyl-(3′ → 5′)-Thymidine1 | B. Juodka; L. Bagdoniene; R. Plaipa |
| 243-253 | Preparation of Oligomeric 2′-Deoxy-5-Fluorouridylate of Defined Length and Backbone Composition: A Novel Pro-Drug form of the Potent Anti-Cancer Drug 2′-Deoxy-5-Fluorouridylate | William H. Gmeiner; Parag Sahasrabudhe; Richard T. Pon; Jacque Sonntag; Shashikumar Srinivasan; Patrick L. Iversen |
| 255-273 | An Efficient Method for the Isolation and Purification of Oligoribonucleotides | Brian Sproat; Francesco Colonna; Bashar Mullah; Dean Tsou; Alex Andrus; Arnold Hampel; Ravi Vinayak |
| 599-605 | Construction of a Translation Enhancer-Containing Vector for Gene Expression in a Prokaryotic Two-Cistron System | Klara R. Birikh; Ekaterina N. Lebedenko; Yuri A. Berlin |
| 607-613 | Structure-Activity Relationship of Phosphonic Acid Analogs of Acyclovir or Ganciclovir Against Human Cytomegalovirus in MRC-5 Cells | John H. Huffman; Robert W. Sidwell; Ann G. Morrison; Jana Coombs; Elmer J. Reist |
| 615-623 | Nucleoside Analogues on the Basis of 4(R),5(R)-Dihydroxymethyl-2-methyl-1,3-dioxolane | Sergey N. Mikhailov; Ekaterina V. Efimtseva; Sergey V. Meshkov; Earl R. Kern |
| 625-636 | A Novel Palladium-Catalyzed Deoxygenation of Guanine O6-Arenesulfonates. A Practicable Synthesis of 2-Aminopurine Nucleosides and Related Analogs | Anton Štimac; Darja Muhič; Jože Kobe |
| 637-655 | 1H NMR Structural Analysis of the Interactions of Proflavine with Self-Complementary Deoxytetranucleosides of Different Base Sequence | D. B. Davies; L. N. Djimant; A. N. Veselkov |
| 657-671 | 1H NMR Thermodynamical Analysis of the Interactions of Proflavine with Self-Complementary Deoxytetranucleotides of Different Base Sequence | D. B. Davies; L. N. Djimant; A. N. Veselkov |
| 673-678 | The Synthesis of 2-Fluoropurine Nucleosides | K. Krolikiewicz; H. Vorbrüggen |
| 679-688 | Synthesis of Bicyclic N4-Oxycytidine Derivatives | D. Loakes; D. M. Brown |
| 689-706 | X-Ray Crystallographic and Kinetic Analysis of Human Purine Nucleoside Phosphorylase Complexes with 1-β-D-Ribofuranosyl-1,2,4-triazole-3-carobxamide and 1-β-D-Ribofuranosyl-1,2,4-triazole-3-carboxamidine | Richard L. Walter; Jindrich Symersky; Anne F. Poirot; Johanna D. Stoeckler; Mark D. Erionf; Steven E. Ealick |
| 707-717 | Synthesis of 3′-Amino and 5′-Amino Hydantoin 2′-Deoxynucleosides | Ahmed A. El-Barbary; Ahmed I. Khodair; Erik B. Pedersen; Claus Nielsen |
| 719-736 | Synthesis of Novel Isothiazole and Isothiazolo[4,5-d] Pyrimidine Analogues of the Natural C-Nucleosides Pyrazofurin and the Formycins | Diederik K. Buffel; Lieven Meerpoel; Suzanne M. Toppet; Georges J. Hoornaert |
| 737-751 | Conjugates of Fluorescein and Saenta (5′-S-(2-Aminoethyl)-N6-(4-nitrobenzyl)-5′-thioadenosine): Flow Cytometry Probes for the ES Nucleoside Transporter Elements of the Plasma Membrane | J. K. Buolamwini; J. D. Craik; J. S. Wiley; M. J. Robins; W. P. Gati; C. E. Cass; A. R. P. Paterson |
| 753-772 | Properties of RecA Complexes with Homopolymeric DNA Strands Depend on Sequence Complementarity. Implications for the Mechanism of Strand Exchange | Mikael Kubista; Bengt Nordén; Masayuki Takahashi |
| 773-798 | Nucleosides. LIV1 Synthesis and Properties of 3′-Azido- and 2′,3′-Dideoxy-6,7-diphenyllumazine Nucleosides | Xiaodong Cao; Wolfgang Pfleiderer |
| 799-809 | Base Changes and Triple-Helix Hybridization Properties of GT Containing Third Strands: A Systematical Study | Jean-Pierre Clarenc; Bernard Lebleu; Jean-Paul Léonetti |
| 811-817 | Synthesis of the Nucleotide Analogue: (R,S)-9-[1-(2-Hydroxyethylthio)-2-phosphonylethyl] Adenine | H. B. Lazrek; H. Khaider; A. Rochdi; J. L. Barascut; J. L. Imbach |
| 819-834 | Chemical-Enzymatic Synthesis of 3′-Amino-2′, 3′-dideoxy-β-D-ribofuranosides of Natural Heterocyclic Bases and Their 5′-Monophosphates | Galina V. Zaitseva; Evgenii I. Kvasyuk; Elena V. Vaaks; Vladimir N. Barai; Sergei B. Bokut; Anatolii I. Zinchenko; Igor A. Mikhailopulo |
| 835-848 | Synthesis of 2′-Deoxyribonucleoside Derivatives of 1-Deazapurine | G. Cristalli; S. Vittori; A. Eleuteri; R. Volpini; E. Camaioni; G. Lupidi |
| 849-880 | Boron Containing Pyrimidines, Nucleosides, and Oligonucleotides for Neutron Capture Therapy | Naganna M. Goudgaon; Geraldine Fulcrand El-Kattan; Raymond F. Schinazi |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 11, Number 9 | |
| 1575-1578 | A Rapid Method for Purification of Oligonucleotides | Ajay Kumar; Hema Dawar; Sudhakar Mathur |
| 1579-1593 | Synthesis of Oligoribonucleotides by the H-Phosphonate Approach Using Base Labile 2′-O-Protecting Groups. V. Recent Progress in Development of the Method | Eriks Rozners; Regina Renhofa; Marina Petrova; Juris Popelis; Viktors Kumpins; Erika Bizdena |
| 1595-1606 | Synthesis and Antiviral Properties of New Cycloalkanol Derivatives of Guanine | S. Halazy; M. Kenny; J. Dulworth; A. Eggenspiller |
| 1607-1620 | 1′, 2′-Seco-2′,3′-Dideoxynucleoside Analogues: Synthesis and Antiviral Evaluation of Racemic Trans-[1′, 5′-Dihydroxy 3′, 4′-methylenylpent-2′-oxy)methyl] Nucleosides | Muhammad Azymah; Claude Chavis; Alain Fruchier; Marc Lucas; Jean-Louis Imbach |
| 1621-1638 | The First Stereocontrolled Synthesis of Thiooligoribonucleotide: (RpRp)- and (SpSp)-UpsUpsU | Zbigniew J. Lesnikowski |
| 1639-1649 | A Dihydropyridine Carrier System for Delivery of 2′,3′-Dideoxycytidine (DDC) to the Brain | Eduardo Palomino; David Kessel; Jerome P. Horwitz |
| 1651-1660 | Synthesis of Thymine Nucleosides Derived from 1-Deoxy-D-psicofuranose | Véronique Faivre-Buet; Annie Grouiller; Gérard Descotes |
| 1661-1666 | Structural Determination of Silicon-Containing Oligonucleotides by 1H-29Si Long-Range Heteronuclear Multiple Quantum Correlation NMR Spectroscopy | James M. Hewitt; William C. Lenhart; Richard N. Moore; Ashis K. Saha; Alexander L. Weis |
| 1667-1671 | Synthesis of an Octameric Phosphodiester of 2, 3-dideoxy-ß-D-erythro-hex-2-eno-pyranosyl-thymine and Its Interactions with Poly-rA and Poly-dA | Eduard Felder; Raphael Gattlen; Flavio Ossola; Gerhard Baschang |
| 1673-1682 | Condensation Reaction Between 2,2-Diphenylthio-2,3-Dideoxyribose and Silylated Pyrimidine Bases | Hiroshi Kawakami; Takashi Ebata; Koshi Koseki; Katsuya Matsumoto; Koji Okano; Hajime Matsushita |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 11, Number 8 | |
| 1445-1453 | Oligonucleotides and Nucleotide-Peptides. LIV. The Synthesis and Hydrolytic Properties of Adenylyl-(5′→Nε)-lysylpeptides — Model Compounds of the AMP-RNA Ligase Covalent Complex | Benediktas Juodka; Sofija Sasnauskiene; Ruta Petniunaite |
| 1455-1461 | RNA Modified Uridines. V. An Improved Synthesis of 3-[3-(S)-Amino-3-carboxypropyl]uridine (acp3U) and Its 5′-Phosphate | Barbara Nawrot; Andrzej Malkiewicz |
| 1463-1466 | An Efficient Synthesis of N2-Isobutyryl-O6-[2-(4-nitrophenyl)ethyl]-5′-O-Dimethoxytrityl-2′-deoxyguanosine | Andrey P. Guzaev |
| 1467-1479 | Efficient Synthesis of 4-Thio-D-ribofuranose and Some 4′-Thioribonucleosides | L. Bellon; J. -L. Barascut; J. -L. Imbach |
| 1481-1488 | Synthesis of Tetrazole Oxathiolane Nucleoside Analogues and Their Evaluation as HIV-1 Antiviral Agents | Philippe Faury; Michel Camplo; Anne-Sophie Charvet; Jean-Claude Chermann; Jean-Louis Kraus |
| 1489-1505 | Synthesis of Racemic Carboacyclonucleosides Derived from Butane-1, 4-Diol and Hexane-1, 6-Diol | Michel Perbost; Marc Lucas; Claude Chavis; Jean-Louis Imbach |
| 1507-1527 | Synthesis, Antiproliferative, and Antiviral Evaluation of Certain Acyclic 6-Substituted Pyrrolo[2,3-D]-pyrimidine Nucleoside Analogs Related to Sangivamycin and Toyocamycin | Eric E. Swayze; William M. Shannon; Robert W. Buckheit; Linda L. Wotring; John C. Drach; Leroy B. Townsend |
| 1529-1537 | An Expeditious Synthesis of Homochiral (R) 2-(9-Purinyl)butane-1, 4-Diols from (S) Butane-1, 2, 4-Triol | Michel Perbost; Marc Lucas; Claude Chavis; Jean-Louis Imbach |
| 1539-1547 | Synthesis of Nucleoside Analogues Containing an Oxetane Ring Fused to the Furan Ring | Robert J. Hambalek; George Just |
| 1549-1559 | A Practical and Stereospecific Approach to the Synthesis of 3′-Deoxy-2′,3′-didehydrothymidine (D4T) | Chandra Vargeese; Elie Abushanab |
| 1561-1574 | Straightforward Synthesis of 6-Thiodeoxyguanosine and Its Incorporation into Oligodeoxynucleotides | Timothy R. Waters; Bernard A. Connolly |
| a-b | Editorial board page for “Nucleosides & Nucleotides”, Volume 11, Number 6 | |
| 1123-1135 | Synthesis and Biological Study of the Cyclopentenyl Carbocyclic Nucleoside Analogue of 5-Azacytidine | Benjamin B. Lim; Victor E. Marquez; Kathryn A. Dobyns; David A. Cooney; Erik De Clercq |
| 1137-1149 | The Synthesis of Novel Regioisomeric Ring-Expanded Xanthine Nucleosides Containing The 5:7-Fused Imidazo[4,5-e][1,2,4]Triazepine Ring System | Vishweshwar S. Bhadti; Anila Bhan; Ramachandra S. Hosmane; Martin Hulce |
| 1151-1173 | Synthesis and Antiviral Activity of Various 5-Substituted 2′-Deoxyuridines and -Cytidines | Dan Peters; Anna-Britta Hörnfeldt; Salo Gronowitz; Nils Gunnar Johansson |
| 1175-1200 | The Synthesis, Structure, and Conformation of 2′-Deoxy Analogues of „Fat“ Xanthine Nucleosides, Containing the Imidazo[4,5-e][1,4]Diazepine Ring System | Anila Bhan; Ramachandra S. Hosmane |
| 1201-1204 | A Convenient Preparation of Protected 2′-0-Methylguanosine | Thomas E. Leonard; Purshotam Bhan; Paul S. Miller |
| 1205-1218 | Synthesis of Some 2′,3′-Dideoxy-2′-C-Methyl-Substituted Nucleosides | Panagiotis Ioannidis; Björn Classon; Bertil Samuelsson; Ingemar Kvarnström |
| 1219-1228 | Synthesis and Anti-Hiv Activity of 3′-0-Formyl Derivatives of Thymidine and 2′-Deoxyuridine | Rakesh Kumar; Edward E. Knaus; Leonard I. Wiebe |
| 1229-1239 | The Crystal and Molecular Structure of the Complex of 2′3′-Didehydro-2′3′-Dideoxyguanosine with Pyridine | Patrick Van Roey; C. K. Chu |
| 1241-1255 | Isotactic Glycero Oligothymidylate. a Convenient Preparation of (R) and (S) 1′, 2′-Seco 2′-Nor Thymidine | Muhammad Azymah; Claude Chavis; Marc Lucas; François Morvan; Jean-Louis Imbach |
| 1257-1261 | N2-Isobutyryl-O6-[2-(p-Nitrophenyl)Ethyl]Guanine: A New Building Block for the Efficient Synthesis of Carbocyclic Guanosine Analogs | Thomas F. Jenny; K. Christian Schneider; Steven A. Benner |
| 1263-1273 | Regioselective 2′/3′-O-Allylation of Pyrimidine Ribonucleosides Using Phase Transfer Catalysis | Vidhya Gopalakrishnan; Vaijayanti Kumar; K. N. Ganesh |
| 1275-1292 | The Identification of 5′-Deoxy-5′-Methylthioguanosine in Human Urine by Gas Chromatography/Mass Spectrometry | William M. Hammargren; Debra R. Luffer; Karl H. Schram; Mark L. J. Reimer; Katsuyuki Nakano; Toshio Yasaka; Allan R. Moorman |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 11, Number 2-4 | |
| xiii | Memorial Issue Honoring Prof. Tohru Ueda | |
| xv-xxvii | Biography | |
| 177-196 | 5′-Hydrogenphosphonates and 5′-Methylphosphonates of Sugar Modified Pyrimidine Nucleosides as Potential Anti-HIV-1 Agents.1 | Alexander A. Krayevsky; Natalie B. Tarussova; Qing-Yu Zhu; Pedro Vidal; Ting-Chao Chou; Penny Baron; Bruce Polsky; Xiang-Jun Jiang; Jasenka Matulič-Adamič; Ivan Rosenberg; Kyoichi A. Watanabe |
| 197-226 | Nucleosides and Nucleotides. 104. Radical and Palladium-Catalyzed Deoxygenation of the Allylic Alcohol Systems in the Sugar Moiety of Pyrimidine Nucleosides§,1 | |
| 227-235 | Nucleosides and Nucleotides. 105. DNA Bending in d(A)4 - d(T)4 TRACTS Containing 3-Deazaadenine or 7-Deazaadenine Substituted for Adenine§,1 | Akira Ono; Chie Ohdoi; Akira Matsuda; Tohru Ueda |
| 237-246 | Nucleosides and Nucleotides. 106. Synthesis and Biological Activity of 1-(2-Deoxy-2-hydroxyimino- or Methoxyimino-β-D-erythro-pentofuranosyl)-thymine and -Cytosine§,1 | |
| 247-260 | Mutation Induced by Deoxyxanthosine in Codon 12 of A Synthetic c-Ha-ras Gene | Hiroyuki Kamiya; Miho Shimizu; Masayuki Suzuki; Hideo Inoue; Eiko Ohtsuka |
| 261-272 | NMR Studies of a DNA Containing 8-Methoxydeoxyguanosine | Yasushi Oda; Seiichi Uesugi; Masaya Orita; Hideo Inoue; Yasutoshi Kawase; Eiko Ohtsuka; Morio Ikeharay |
| 273-278 | Formation of an Unexpected 2-Deoxy-α-D-Threo-Pentofuranosyl Azide by Reaction of O2,3′-Anhydro-5′-O-trityl-2′-deoxycytidine with Lithium Azide | I. A. Mikhailopulo; G. V. Zaitseva; E. V. Vaaks; H. Rosemeyer; F. Seela |
| 279-293 | The Synthesis of Novel Carbohydrates Amenable to the Synthesis of 2′,3′-Dideoxy-3′-Branched Nucleosides | Jeffrey S. Pudlo; Leroy B. Townsend |
| 295-310 | Synthesis and Biological Action of a New Cyclic AMP Analogue | Toshiaki Fujihashi; Takahiro Ogata; Tetsuo Ohkuma; Tohru Endo; Akira Kaji |
| 311-317 | Quantification Analysis of Human α- and δ-Globin Genes. Mutations in 5′-Splice Junction Sequence and α- and δ- Thalassemias | Yôichi Iida |
| 319-328 | Synthesis of 6-Methyluridine via Palladium-Catalyzed Cross-Coupling Between A 6-Iodouridine Derivative and Tetramethylstannane | Hiromichi Tanaka; Hiroyuki Hayakawa; Sachiko Shibata; Kazuhiro Haraguchi; Tadashi Miyasaka; Kosaku Hirota |
| 329-340 | Synthesis of 2′,3′-Dideoxy-2′-methylene Pyrimidine Nucleosides as Potential Anti-Human Immunodeficiency Virus (HIV) Agents | Tai-Shun Lin; Mei-Zhen Luo; Mao-Chin Liu |
| 341-349 | A Convenient and Stereoselective Synthesis of 2′-Deoxy-β-L-Ribonucleosides | Shizuyoshi Fujimori; Naoko Iwanami; Yuichi Hashimoto; Koichi Shudo |
| 351-363 | The Controlled Stereospecific Reduction of Cyclopentenyl Cytosine (CPE-C) to Carbodine and Isocarbodine | Pamela L. Russ; Lajos Hegedus; James A. Kelley; Joseph J. Barchi Jr.; Victor E. Marquez |
| 365-372 | Oxidative Cyclization of 2′,3′-O-Isopropylidene-Adenosines into 5′-O,8-Cycloadenosines with Lead Tetraacetate: Remarkable Effect of N6-Substituents on the Oxidation | Yukio Kitade; Tohru Makino; Kosaku Hirota; Yoshifumi Maki |
| 373-382 | Synthetic Nucleosides and Nucleotides. XXX.1 Synthesis and Antiviral Activity of 3′-Azido, 2′,3′-Unsaturated and 2′,3′-Dideoxy Derivatives of E-5-Styryl-2′-Deoxyuridine on Human Immunodeficiency Virus | Toyofumi Yamaguchi; Mineo Saneyoshi |
| 669-678 | Synthesis of Oligodeoxyribonucleotide Analogues by Use of Deoxyribonucleoside-3′-yl O-bis(1,1,1,3,3,3-Hexafluoro-2-Propyl) Phosphites as New Key Intermediates | Hideo Hosaka; Yoshikazu Suzuki; Hiroyuki Nakamura; Hidenori Funakoshi; Hideki Nakashima; Naoki Yamamoto; Hiroshi Takaku |
| 679-691 | Synthesis of Adenosine, Guanosine and Cytidine Monomer Building Units Bearing the [[2-(Methylthio)-phenyl]thio]methyl (MPTM) Group as The 2′-Hydroxyl Protecting Group | Mitsuo Sekine; Takashi Nakanishi |
| 693-705 | Practical Synthesis of AZT and AZDU from Xylose: Efficient Deoxygenation via Nucleoside 2′-Xanthates | Yaoquan Chen; John G. Bauman; Chung K. Chu |
| 707-718 | Synthesis and Biological Evaluation of 9-(f-2, c-3-Bishydroxymethyl-r-cyclopropylmethyl)-9H-adenine (A Lower Methylene Homolog of Carbocyclic Oxetanocin) and Related Compounds | Nobuya Katagiri; Hiroshi Sato; Chikara Kaneko |
| 719-730 | Recognition of the Nucleoside in the First Position of the Anticodon of Isoleucine tRNA by Isoleucyl-tRNA Synthetase from Escherichia Coli | Tomonari Muramatsu; Tatsuo Miyazawa; Shigeyuki Yokoyama |
| 731-738 | Conformation Analysis of Two Anti-HIV Nucleoside Analogues 2′,3′-Dideoxy-3′-fluorocytidine and Its N4-Dimethylaminomethylene Prodrug Derivative | Vivian Cody; Thomas I. Kalman |
| 739-748 | Synthesis of 1′,2′-Seco-nucleoside Analogues of AZT | Purushotham Vemishetti; Hussein I. El Subbagh; Elie Abushanab; Raymond P. Panzica |
| 749-757 | O-Alkylation of Dialkyl Phosphates and O-Alkyl Phosphonates via the Stannyl Intermediates | Shokichi Ohuchi; Takashi Imada; Tsujiaki Hata |
| 759-771 | Conformational Rigidity of N4-Acetyl-2′-O-methylcytidine Found in tRNA of Extremely Thermophilic Archaebacteria (Archaea) | Gota Kawai; Takeshi Hashizume; Masayuki Yasuda; Tatsuo Miyazawa; James A. McCloskey; Shigeyuki Yokoyama |
| 773-785 | Divalent Metal Ion-Catalyzed Pyrophosphate Bond Formation in Aqueous Solution. Synthesis of Nucleotides Containing Polyphosphate | H. Sawai; M. Shimazu; H. Wakai; H. Wakabayashi; K. Shinozuka |
| 787-819 | Nucleosides. IL. Synthesis and Properties of 2,4-Quinazolinedione N-1-2′ Deoxy-, 3′-Deoxy- and 2′,3′-Dideoxynucleosides | Martin Dunkel; Wolfgang Pfleiderer |
| 821-834 | Nucleic Acid Related Compounds. LXXXI. Efficient General Synthesis of Purine (Amino, Azido, and Triflate)-Sugar Nucleosides | Morris J. Robins; S. D. Hawrelak; Amelia E. Hernández; Stanislaw F. Wnuk |
| 835-853 | Molecular Conformation of 2′-Deoxy-2′-methylidene-cytidine: A Potent Antineoplastic Nucleoside | Yuriko Yamagat; Ken-ichi Tomita; Nobuhiro Marubayashi; Ikuhiko Ueda; Shinji Sakata; Akira Matsuda; Kenji Takenuki; Tohru Ueda |
| 855-864 | Synthesis of Methylenecyclobutyl- and Cyclobutenyl Adenine, Potent Antiviral Carbocyclic Analogues of Oxetanocin A | Tokumi Maruyama; Yasuaki Hanai; Yoshiko Sato |
| 865-887 | Studies on Griseolic Acid Derivatives X. Synthesis and Phosphodiesterase Inhibitory Activity of 2-Substituted Derivatives of Griseolic Acid | Masakatsu Kaneko; Misako Kimura; Yoshinobu Murofushi; Takashi Yasumoto; Yasuteru Iijima; Mitsuo Yamazaki |
| 889-901 | Spin-Labeled Oligonucleotides Site Specifically Labeled at the Internucleotide Linkage. Separation of Stereoisomeric Probes and EPR Spectroscopical Detection of Hybrid Formation in Solution | Shunji Nagahara; Akira Murakami; Keisuke Makino |
| 903-945 | Nucleoside Analogues as Chemotherapeutic Agents: A Review | C. Périgaud; G. Gosselin; J. L. Imbach |
| 947-956 | Syntheses of Phosphonate Analogues of Dideoxyadenosine (DDA)-, Dideoxycytidine (DDC)-, Dideoxyinosine (DDI)-, and Deoxythymidine (DDT)-5′-Monophosphates | John A. Secrist III; Robert M. Riggs; Robert N. Comber; John A. Montgomery |
| a-b | Editorial board page for “Nucleosides & Nucleotides”, Volume 11, Number 1 | |
| 1-9 | Structural Features Of 2′,3′-Riboanhydroadenosine, A Conformationally Restricted Termination Substrate Of DNA Polymerases | Galina Gurskaya; Alexey Bochkarev; Alexander Zdanov; Alexander Papchikhin; Alexander Krayevsky |
| 11-21 | Synthesis and Anti-HIV Activity of a New Hexopyranoside Analogue of AZT | Ferenc Sztaricskai; Zoltán Dinya; Gyula Batta; Lajos Gergely; Béla Szabó |
| 23-35 | Utilization of 2′-Deoxy-6-thioguanosine 5′-Triphosphate In DNA Synthesis Catalyzed by DNA Polymerase I Klenow Fragment of Escherichia Coli | Yi-He Ling; J. Arly Nelson; David Farquhar; Kenneth L. Beattie |
| 37-47 | Reactions Of 2′-Deoxy-2′-halouridines and O2,2′-Cyclouridine with Lithium Dialkylamides: Formation of 1′,2′-Unsaturated Derivatives | Atsushi Kittaka; Hiromichi Tanaka; Tadashi Miyasaka; Kentaro Yamaguchi |
| 49-60 | Synthesis Of 6-Alkoxy-5-bromo-5,6-dihydropyrimidine Nucleosides Using Dibutyltin Alkoxide-Bromine | A. George Samuel; Hari Babu Mereyala; K. N. Ganesh |
| 61-83 | Synthesis of the Pyrido[4,3-D]pyrimidine Congeners of Inosine and of Adenosine - A New Class of 6:6 Bicyclic C-Ribofuranosides | Kambhampati V. B. Rao; Robert S. Klein; Mallela S. P. Sarma; Brian A. Otter |
| 85-95 | Synthesis of Protected 8-Substituted Deoxyribonucleosides and Its Helix Stability in Oligodeoxyribonucleotides Containing the Eco RI Recognition Site | Hiroshi Komatsu; Takashi Ichikawa; Michiaki Nakai; Hiroshi Takaku |
| 97-119 | Synthesis Of 9-(1-Deoxy-1-phosphono-β-D-psicofuranosyl)-1,9-dihydro-6H-purin-6-one as a Potential Transition State Analog Inhibitor of Purine Nucleoside Phosphorylase | Robert D. Elliott; Shri Niwas; James M. Riordan; John A. Montgomery; John A. Secrist III |
| 121-139 | Reaction of 5-αChloroacetyl-4-glycosylaminopyrimidines with Thiourea. Synthesis of 4-Glycosylaminofuro[2,3-d]pyrimidines and 4-Glycosylamino-5-(2-amino-4-thiazolyl)pyrimidines | M. L. Quijano; M. Nogueras; A. Sánchez |
| 141-156 | Stereoselective Synthesis of Ribonucleoside 3′,5′-Cyclic Methyl(phenyl)phosphonates and Phosphonothioates | H. C. P. F. Roelen; E. de Vroom; A. H. J. Wang; G. A. van der Marel; J. H. van Boom |
| 159-166 | Computer Graphics Modelling and Molecular Dynamics Simulation of the Core of the Self Splicing Intervening Sequence of the T4 NrdB mRNA in the Presence of the Guanosine Cofactor | Lenoart Nilsson; Agneta Ahgren-Stålhandske; Ann-Sofie Sjögren; Solveig Hahne; Britt-Marie Sjöberg |
| 167-173 | Free Energy Calculations Predict Sequence Specificity in DNA-Drug Complexes | T. Härd; L. Nilsson |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 10, Number 8 | |
| 1625-1640 | Structure and Conformation of 5′-Chlorocyclocytidine, a Potent Inhibitor of Nucleic Acid Synthesis: X-Ray, 1H and 13C NMR Analyses | George I. Birnbaum; Miloś Budéšínsk; Ladislav Novotn |
| 1641-1655 | Thiopurine Nucleosides: Variations in Hydrophobicity Among Nl Suhstituents | Peter C. Ratsep; Nrusingha C. Mishra; Arthur D. Broom |
| 1657-1665 | Synthesis of N-Aminopyrazinium Analogs of Cytidine and 2′-Deoxycytidine | Miroslav Bobek; Pittaya Tuntiwachwuttikul; M. Mohsen Ismail; Thomas J. Bardos |
| 1667-1675 | Covalent Nucleoside Adducts of Aspidosperma Alkaloids | B. Danieli; G. Lesma; G. Palmisano; D. Passarella; B. Pyuskyulev |
| 1677-1692 | Inhibition and Substrate Specificity of Adenosine Deaminase. Interaction with 2′-, 3′- and/or 5′-Substituted Adenine Nucleoside Derivatives | G. Maury; T. Daiboun; A. Elalaoui; C. Génu-Dellac; C. Périgaud; C. Bergogne; G. Gosselin; J. -L. Imbach |
| 1693-1706 | Synthesis of Ring-Expanded Xanthines and Xanthosines Containing the Imidazo[4,5-d][1,3]diazepine Ring System | Ramachandra S. Hosmane; Vijayvithal P. Vaidya; Mi Kyung Chung; Upali Siriwardane; Hongming Zhang; Narayan S. Hosmane |
| 1707-1717 | Synthetic Studies on the Isomeric N -Methyl Derivatives of C-Ribavirin | Giin-Yuan Shen; Roland K. Robins; Ganapathi R. Revankar |
| 1719-1728 | Synthesis of 4-Substituted Pyrimidine 2′,3′-Dideoxynucleosides | L. De Napoli; A. Messere; D. Montesarchio; G. Piccialli; C. Santacroce |
| 1729-1742 | Effect of 2-Amino Substitution on the Antiviral Effects of 5-Ethyl-2′-Deoxyuridine and (E)-5-(2-bromovinyl)-2′-Deoxyuridine and Their Incorporation into DNA | J. Sági; A. Szabolcs; K. Ebinger; L. Ötvös; J. Balzarini; E. De Clercq |
| 1743-1757 | Synthesis and Biological Properties of 2-Amino-3-fluoro-2,3-Dideoxy-D-Pentofuranosides of Natural Heterocyclic Bases | Igor A. Mikhailopulo; Grigorii G. Sivets; Tamara I. Pricota; Nicolai E. Poopeiko; Jan Balzarini; Erik De Clercq |
| 1759-1769 | Imidazole Ring Opening of 7-Methylguanosine at Physiological pH | G. Barbarella; V. Tugnoli; M. Zambianchi |
| 1771-1787 | Synthesis and Biological Evaluation of Some D-Xylofuranosyl-Pyridine C-Nudeosides | F. Verberckmoes; E. L. Esmans; R. A. Dommisse; J. A. Lepoivre; F. C. Alderweireldt; J. Balzarini; E. De Clercq |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 10, Number 7 | |
| 1431-1449 | Synthesis And Antiviral Evaluation Of 2′,3′-Secothymidine Analogs of ddT and AZT | Annie-Fransoise Maggio; Valerie Boyer; Anne-Marie Aubertin; Georges Obert; André Kirn; Jean-Louis Imbach |
| 1451-1463 | Synthesis and Biological Activity of 5-halo-2-Pyrimidinone 3′-Azido-2′,3′-Dideoxyribosides | S. M. N. Efange; A. K. Dutta |
| 1465-1475 | Phosphonoformate Esters of Anti-HIV Nucleosides: 3′-Azido-3′-deoxythymidine and 2′,3′-Dideoxycytidine Derivatives Containing a Small 5′-(0-Alkoxycarbon-ylphosphinyl) or 5′-(O-Cholesterylcarbonylphosphinyl) Substituent | Jayanta Saha; Ruth M. Ruprecht; Andre Rosowsky |
| 1477-1483 | A Direct and Efficient Synthesis of 5′-Deoxy-2′, 3′- | James G. Davidson; Phillip J. Fiore |
| 1485-1498 | Synthesis of a Non-Hydrolyzable Dinucleoside Analogue | Stephen H. Kawai; George Just |
| 1499-1505 | Strategy for Industrial Scale Production of Dideoxyinosine: Enzymatic Deamination of Dideoxyadenosine by Adenosine Deaminase | Carol M. Beach; Robert K. Evans; Mary Sue Coleman |
| 1507-1524 | N2-Substituted-2′-deoxyguanosine 5′-Triphosphates as Substrates for E. coli DNA Polymerase I | Stephen Freese; Jörg Hoheisel; Hans Lehrach; George Wright |
| 1525-1549 | Synthesis of 2′-Deoxy-2′ -Fluoro-D-Arabinopyranopyranosyl Nucleosides and Their 3′,4′-Seco analogues | P. Herdewijn; A. Van Aerschot; R. Busson; P. Claes; E. De Clercq |
| 1551-1562 | Synthesis and Evaluation of Anti-HIV-1 and Antitumor Activity of 2′,3′-didehydro-2′,3′-dideoxy-3-deazaadenosine, 2′,3′-dideoxy-3-Deazaadenosine and Some 2′,3′-dideoxy-3-deaza-adenosine 5′-dialkyl Phosphates1 | P. Franchetti; L. Cappellacci; G. Cristalli; M. Grifantini; A. Pani; P. La Colla; G. Nocentini |
| 1563-1572 | Coronary Vasoactivity of Novel N6-Substituted Adenosines | Shozo Kusachi; Robert D. Thompson; William J. Bugni; Nobuyuki Yamada; Ray A. Olsson |
| 1573-1598 | Synthesis and Biological Evaluation of 2-(2-Deoxy-D-erythro-pent-1-enofuranosyl)pyridine C-Nucleosides | E. De Vos; E. L. Esmans; J. A. Lepoivre; F. C. Alderweireldt; R. A. Dommisse; P. François; R. Touillaux; J. Balzarini; E. De Clercq |
| 1599-1614 | 3′/5′-Regioselectivity of Introduction of the 9-Fluorenyl-Methoxycarbonyl Group to 2′-o-Tetrahydropyran-2-YL-and 2′-O-(4-Methoxytetrahydropyran-4-YL-)-Nucleosides: Useful Intermediates for Solid-Phase-Rna-Synthesis | Christian Lehmann; Yao-Zhong Xu; Chris Christodoulou; Michael J. Gait; Luc Van Meervelt; Madeleine Moore; Olga Kennard |
| 1615-1624 | The Synthesis of Some 5-Vinyluracil-Nucleoside Analogues | R. F. Whale; P. L. Coe; R. T. Walker |
| a | Editorial Board Page for “Nucleosides & Nucleotides”, Volume 10, Number 4 | |
| 739-753 | Synthesis and Antiherpetic Activities of Several Acyclic Analogues Of Guanosine | Hirofumi Furusho; Takahiro Ogata; Akihisa Kato; Yoshie Sato; Tohru Endo; Akira Kaji |
| 755-761 | An Improved Method for The Preparation Of The Phosphoramidites Of Modified 2′-Deoxynucleotides: Incorporation Of 8-Oxo-2′-Deoxy-7H-Guanosine Into Synthetic Oligomers | Veeraiah Bodepudi; Charles R. Iden; Francis Johnson |
| 763-779 | Synthesis of Modified Nucleosides. Palladium-Catalysed Couplings of Organostannanes or Organoboranes with Pyrimidine Nucleosides | Bernard L. Flynn; Vilma Macolino; Geoffrey T. Crisp |
| 781-798 | Synthesis of 9-(2-Deoxy-2-Fukuoro-β-D- Abinoruranosyl)Hypoxhine. The First Direct Introduction of A 2′-β-Fldoro Substituent in Ppepormed Purine Nucleosides. Studies Directed Toward the Synthesis of 2′-DEOXY-2′-Substituted Arabppmocebosides. 8.1 | Jacek Krzeminski; Barbara Nawrot; Krzysztof W. Pankiewicz; Kyoichi A. Watanabe |
| 799-817 | Nucleosides, XLVIII. Syntheses and Properties of Quinazoline N-1-Ribofuranosides | Martin Dunkel; Wolfgang Pfleiderer |
| 819-836 | Synthetic, Structural, and Conformational Studies of Methylated Ring-Expanded Nucleosides Containing the Ihidazo[4, 5-e][1, 4]Diazepine Ring System | Ramachandra S. Hosmane; Anila Bhan; Martin Hulce; Hongming Zhang; Narayan S. Hosmane |
| 837-851 | Synthesis of the 2′-,3′-Didehydro-2′-,3′-dideoxy and 2′-,3′-Dideoxy Derivatives of 6-Azauridine and a New Route to 2′-,3′-Didehydro-2′-,3′-dideoxy-5-chlorouridine | Andre Rosowsky; Niranjan N. Pai |
| 853-866 | Synthesis of Bridged Pyrimidine Nucleosides and Triazo [4, 3-c] Pyrimidine Nucleoside Analogues | Stefania Barbato; Gennaro Piccialli; Ciro Santacroce; Lorenzo De Napoli; Luciano Mayol |
| 867-882 | Solid-Phase Synthesis of Oligodeoxyribonucleotide Analogues Containing 5, 6-Dihydroimidazo [1, 2-c] Pyrimidin-5-One as a Base Moiety | Stefania Barbato; Gennaro Piccialli; Ciro Santacroce; Lorenzo De Napoli; Luciano Mayol |
| 883-894 | Synthesis and Biological Evaluation of 4-Carbamoyl-2-β-D-Ribofuranosyl-Pyridine | Pieter E. Joos; Eddy L. Esmans; Roger A. Dommisse; Walter Van Dongen; Jozef A. Lepoivre; Frank C. Alderweireldt; Jan Balzarini; Erik De Clercq |
| 895-909 | Introduction of 5′-Terminal Amino and Thiol Groups into Synthetic Oligonucleotides | R. K. Gaur |
| 911-912 | Erratum | |
| 913 | Erratum | |
| 409-412 | Base-Modifled Purine 2′,3′-Dideoxyribonucleosjdes: Synthesis via Deoxygenation or Direct Nucleobase Anion Glycosylation | F. Seela; H. Rosemeyer; R. Gumbiowski; K. Mersmann; H.-P. Muth; A. Röling |
| 413-414 | A Simple Preparation of 5′-Biotinylated Oligonucleotides and Their use as Primers in Dideoxy-Sequencing of DNA | Anthony J. Cocuzza; Robert J. Zagursky |
| 415-418 | Properties of Trialkoxysilyl Grows | Wojciech T. Markiewicz; Katarzyna Adrych-Rozek |
| 419-422 | Anti-HIV Activity of the Antisense Oligonucleotides Bearing Lipophilic and Alkylating Groups at the 5′-Terminus | T. V. Abramova; V. M. Blinov; V. V. Vlassov; V. V. Gorn; V. F. Zarytova; E. M. Ivanova; D. A. Konevets; O. A. Plyasunova; A. G. Pokrovsky; L. S. Sandahchiev; F. P. Svinarchuk; V. P. Starostin; S. R. Chapligina |
| 423-426 | Stereoselective Synthesis of 2′,3′-Dideoxy-and 2,3′-Didehydro-2′,3′-dideoxy-nucleosides | Chung K. Chu; J. Warren Beach; J. Ramesh Babu; Lak Shin Jeong; Heaok Kim; Jeong; Soon Kil Ahn; Qamrul Islam; Sang Joa; Yaoquan Chen |
| 427-430 | 9-[2-(Phosphonomethoxy)alkoxy]purines, A New Series of Antiviral Acyclonucleotides | D. M. Duckworth; M. R. Harnden; R. M. Perkins; D. N. Planterose |
| 431-455 | Biologically Important Nucleosides: A General Method for the Synthesis of Unsaturated Ketonucleosides of Uracil and its Analogs | Dimitri Komiotis; Sylvie Delatre; Leonard Holt; Abraham P. Ollapally; Jan Balzariei; Erik De Clercq; Masaaki Iigo |
| 457-460 | Abasic Oligodeoxyribonucleoside Phosphorothioates as Inhibitors of the Human Immunodeficiency Virus-1 (HIV-1) Phosphorothioate Inhibition of HIV-1 Reverse Transcriptase and Interactions with Syrian Hampster Fibroblast (V79) Cells | William Egan; Jila Boal; Radhakrishnan P. Iyer; Christy Storm; Samuel H. Wilsont; Anita Meyer; Patrick Iversenq |
| 461-464 | Preparation and Properties of Oligodeoxynucleoside Phosphorodithioates | Kirsten Bjergarde; Bjarne H. Dahl; Otto Dahl |
| 465-468 | Enzymatic Sywmesis of Dideoxyribonucleosides | D. Betbeder; C. M. Heath; D. U. Hutchinson |
| 469-475 | Oligonucleotide Analogues with Terminal 3′-3′- and 5′-5′-Internucleotidic Linkages as Antisense Inhibitors of Viral Gene Expression | H. Seliger; A. Fröhlich; M. Montenarh; J. F. Ramalho Ortigao; H. Rösch |
| 479-481 | 3′/5′-Regioselectivity of Introduction of the 9-Fluorenyl-Methoxycarbonyl Group to 2′-O- Tetrahydropyran-2-Yl- and 2′-O-(4- methoxytetrahydropyran-4-Yl-)-nucleosides Useful Intermediates for Solid-Phase-RNA-Synthesis | Christian Lehmann; Yao-Zhong Xu; Chris Christodoulou; Michael J. Gait; Luc Van Meervelt; Madeleine Moore; Olga Kennard |
| 483-485 | Phosphonate Isosteres of Acyclovir and Ganciclovir Honophosphates Synthesis and Anti-Herpesvirus Activity | Choung Un Kim; Bing Y. Luh; Peter F. Misco; John C. Martin |
| 487-490 | Synthesis and Biological Evaluation of Carbocyclic Analogues of Ribavirin | Stewart A. Noble; Nicola E. Beddall; Alison J. Beveridge; Clara L.P. Marr; Chi L. Mo; Peter L. Myers; Charles R. Penn; Richard Storer; Jacqueline M. Woods |
| 491-493 | Synthesis of Some 2′,3′-Didehydro-2′,3′-dideoxynucleosides and 2′,3′- dideoxynucleosides | Pawel Serafinowski |
| 495-496 | Solid Phase -Nucleotide Links Cleavable by Mild Acid Treatments: Phosphoramidates, Phosphoesters and Ethers | Eduard R. Felder |
| 497-498 | Novel Analogues of the Nucleoside Antibiotics Coroyepin | Vasu Nalr; David F. Purdy; Arthur G. Lyons |
| 499-500 | Metal Mediated Reactions in Nucleside Synthesis | Vasu Nalr; Todd B. Sells |
| 501-502 | Novel Inhibitor-Probes of DNA Polymerase III Based on DGTP Analogues of the H2·HPURA Type: Redesign of the Inhibitor Structure Using an N2-Benzylguanine Format | M. Butler; L. W. Dudycz; N. N. Khan; G. E. Wright; N. C. Brown |
| 503-505 | The Synthesis and Interaction of Novel GTP Derivatives with Ras Oncogene Proteins | Timothy P. Noonan; Lech W. Dudycz; George E. Wright |
| 507-509 | Biotinylation of Oligonucleotides and Their Use as Polymerase Chain Reaction Primers | M. Bengtström; L. Harju; A-C. Syvhen |
| 511-514 | Some Chemical and Stereochemical Aspects of Ribonucleoside H-Phosphonate and H-Phosphonothioate Diester Synthesis | Jacek Stawinski; Roger Stromberg; Mats Thelin |
| 515-516 | Studies on the Conversion of Nucleoside H-Phosphonate Monoesters into the Corresponding H-Phosphonothioates | Jacek Stawinski; Roger Stromberg; Rula Zain |
| 517-518 | Studies on Sulfurization of Nucleoside H-Phosphonate and H-Phosphonothioate Esters Using 3H-1,2-Benzodithiol.3-one 1,1-dioxide | Jacek Stawinski; Mats Thelin; Erik Von Stedingk |
| 519-520 | Ribonucleoside H-Phosphonates. Pyridine vs Quinoline - Influence on Condensation Rate | J. Stawinski; R. Strömberg; E. Westman |
| 521-522 | 2,3′-Anhydro-[l- (6′- O-benzoyl-2′,5′- dideoxy-β-D-glucofuranosyl)thymine], a Versatile Starting Material for Homo - Nucleosides | Johann Hiebl; Erich Zbiral; Jan Balzarinib; Eric De Clercq |
| 523-525 | Oligonucleotide Derivatives in Organism: Distribution Among Organs, Rates of Release and Degradation | O. M. Bazanova; V. V. Vlassov; V. F. Zarytova; E. M. Ivanov; E. A. Kuligina; L. A. Yakubov; M. N. Abdukayumov; V. N. Karamyshev; G. Zon |
| 527-529 | More Efficient Alkylating Oligonucleotide Derivatives for the Sequence Specific Chemical Modification of dsDNA | V. V. Vlassov; A. A. Godovikov; A. A. Gall; E. M. Ivanova; A. U. Semeryanova |
| 531-533 | The Chemical Synthesis of ATP-Derivative of Phosphoglyceric Acid | Lucyna A. Wozniak; Halina Serafinowska; Colin B. Reese |
| 535-536 | Inhibition of the Reverse Transcriptase of HIV-1 by 3′-Azidothymidine Triphosphate and 3′-Azido-oligothymidylate | Olaf Heidenreich; Fritz Eckstein |
| 537-539 | Nuclear Accumulation of Microinjected Antisense Oligonucleotides | Jean Paul Leonetti; Nadir Mechti; Geneviève Degols; Bernard Lebleu |
| 541-542 | Ethidium Oligodeoxynucleotide Derivatives. Stability Against Cellular Nuclease Hydrolysis and Photochemical Modification of Cellular Proteins in the Living Cells | A. A. Koshkin; A. V. Lebedev; A. S. Ryte; V. V. Vlassov |
| 543-545 | Synthesis of 3-Deazaclitocwe [2-Amino-3-nitro-4-(β-D-ribofuranosylamino)pyridine] as Cytotoxic Agent | Palmarisa Franchetti; Loredana Cappellacci; Gloria Cristalli; Mario Grifantini; Sauro Vittori |
| 547-548 | Interaction of a Minor Groove Binder with a Fluorescent DNA Oligomer Containing the Eco RI Recognition Sequence | N. Patel; A. Grälund; H. Berglund; L. Nilsson; R. Rigler; L. W. McLaughlin |
| 549-551 | Synthesis, Physical, Chemical, and Enzyme Studies on bis-2,β-Diaminopurine β-D-Ribofuranoside p1, p4-Tetraphosphate | G. Michael Blackburn; Mao-Jun Guo |
| 553-554 | Synthesis of Oligodeoxynucleoside Phosphorodithioates by a Phosphortriester Method | Bjame H. Dahl; Kirsten Bjerghde; John Nielsen; Otto Dahl |
| 555-561 | Synthesis of Base Modified Phosphorothioate Oligodeoxynucleotides as Inhibitors of HIV-1 | O. Kemal; T. Brown; S. Burgess; J. D. Bishop; A. J. Leigh-Brown |
| 563-564 | Hydrogen Fluoride Mediated Alkylation and Dimerization of the Base Moiety of the cis Diastereoisomers of 5,6-Dihydroxy-5,6-dihydrothymidine | Michel Polverelli; Maurice Berger; Jean Cadet |
| 565-566 | Synthesis of Oligodeoxynucleotides Bearing a Radiation Induced DNA Damage: Deoxyribosylurea and Deoxyribosylformamide | André Guy; Hervé Bazin; Robert Teoule |
| 567-568 | Conformation of 3′-Substituted 2′,3′-Dideoxyribonucleosides in Aqueous Solution; Nucleoside Analogues with Potential Antiviral Activity | Pentti Oksman; Ryszard Stolarski; Alex Azhayev; Harri Lönnberg |
| 569-570 | Interconversion and Hydrolysis of Monoalkyl Esters of Adenosine 2′- and 3′-Monophosphates: Kinetics and Mechanisms | Mikko Oivanen; Ralf Schnell; Wolfang Pfleiderer; Harri Lönnberg |
| 571-572 | Kinetics and Mechanism for Acid-Catalyzed Hydrolysis of Regioisomeric 2′-Deoxyribonucleosides of 8-Azaadenine and Substituted Benzotriazoles | Rainer Käppi; Zygmunt Kazimierczuk; Frank Seela; Harri Lönnberg |
| 573-574 | A New Support For Automated Oligonucleotide Synthesis | Christie McCollum; Alex Andrus |
| 575-577 | Synthesis and Properties of Daunomycin Mono- and Oligonucleotide Derivatives | V. F. Zarytova; T. S. Godovikova; T. V. Maltseva; D. S. Sergeyev |
| 579-580 | Investigation of the C-Myc and C-Fos Genes Functions with Retroviral Vectors Producing Antisense RNA | V. V. Vlassov; F. P. Svinarohuk; D. A. Konevets; E. J. Frolova; M. Markelov; V. A. Lavrovsky; A. Ustinov |
| 581-582 | Interaction of Oligonucleotide Derivativts with Animal Cells | V. V. Vlassov; E. A. Deeva; M. N. Nechaeva; E. N. Rykova; L. A. Yakubov |
| 583-584 | Synthesis of Thymidine Analogues with a Cyanoimido Substituent | P. Wigerinck; A. Van Aerschot; L. Kerremans; J. Balzarini; E. De Clercq; P. Claes; P. Herdewijn |
| 585-586 | 5-(Thien-2-yl)-2′-deoxyuridine: A New and Potent Inhibitor of Herpes Simplex Virus Type 1 Replication | P. Wigerinck; A. Van Aerschot; E. De Clercq; P. Herdewijn |
| 587-588 | Sugar Modified Oligonucleotides | K. Augustyns; A. Van Aerschot; P. Herdewijn |
| 589-590 | Synthesis and Anti-HIV Activity of Dideoxycytidine Analogues Containing a Pyranose Carbohydrate Moiety | A. Van Aerschot; L. Kerremans; J. Balzarini; E. De Clercq; P. Herdewijn |
| 591-592 | Synthesis and Antiviral Activity of 1.4-Dioxane, 1.4-Oxathiane and 1,4-Morpholine Nucleoside Analogues | A. Van Aerschot; J. Balzarini; E. De Clercq; P. Herdewijn |
| 593-594 | Intermolecular Association of Deoxycytidylyl-(3′,5′)deoxy-guanosine and Thymidylyl-(3′,5′)-deoxyadenosine in Dimethylsulfoxide | Giovanna Barbarella; Luisa Tondelli; Vitaliano Tugnoli |
| 595-597 | Synthesis and Application of N(6)-Phenoxycarbonyl-deoxy-adenosine Derivatives in Oligonucleotide Probes Chemistry | Edyta Krzymańska-Olejnik; Ryszard W. Adamiak |
| 599-600 | First, Solid Support-Aided Introduction of Isopentyladenosine, Hypermodified Nucleose of TRNA, into Oligoribonucleotide Chain | Piotr Sacute; widerski; Wieslaw Z. Antkowiak; Ryszard W. Adamiak |
| 601-602 | Silyloxyphosphanes. New Phosphitylating Reagents in Nucleotide Chemistry | W. Dabkowski; J. Michalski; Q. Wang |
| 603-605 | X-Ray Crystal Structure of Luminarine - Aglycone of Highly Fluorescent Luminarosine | Dorota A. Adamiak; K. Surma; Marian Gawron; Bohdan Skalski |
| 607-608 | Mechanism of Initiation of Transcription in Escherichia Coli | Rakesh K. Mishra; Dipankar Chatteji |
| 609-613 | Sequence Specific Chemical Recognition Of DNA | Jyoti Mehrotra; Krishna Misra; Rakesh K. Mishra |
| 615-617 | Synthesis of Aryl Phosphorodichloridothioates from ARYL Phosphorodichloridites via Arbuzov-Type Rearrangement | Antonio Procopio; Giovanni Sindona; Nicola Uccella |
| 619-620 | Synthesis of Nucleosides Using Trimethylsilyl Perfluoroethoxyethanesulphonate as Catalyst | J. A. Maurinsš; J. J. Jansons; M. J. Lidaks |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 9, Number 4 | |
| 479-488 | The Effect of Exocyclic Substituents on Base-Pair Propeller Twist | C. C. Wilson |
| 489-497 | Pseudo-ADP: Darstellung und Biomimetische Eigenschaften | Martina Kinzig; Karl-Siegfried Boos |
| 499-513 | Crystal and Molecular Structures of the Antiviral Acyclonucleoside 9-[4-Hydroxy-3-(hydroxymethyl)butyl]guanine (BRL 39123, Penciclovir) and its Prodrug 9-[4-Acetoxy-3-(acetoxymethyl)butyl]-2-aminopurine (BRL 42810, Famciclovir) | Michael R. Harnden; Richard L. Jarvest; Alexandra M. Z. Slawin; David J. Williams |
| 515-531 | Dinucleoside Phosphates Containing Arabinose or Deoxyxylose. Hydrolysis by Exonucleases and Stacking Properties | N. I. Sokolova; N. G. Dolinnaya; N. F. Krynetskaya; Z. A. Shabarova |
| 533-546 | Aldol Reaction of Nucleoside 5′-Carboxaldehydes with Acetone. Synthesis of 5′-C-Chain Extended Thymidine Derivatives | María-José Camarasa; Federico G. De las Heras; María Jesús Pérez-Pérez |
| 547-557 | Synthesis and Structure of 2′,3′-Dideoxy-3′-fluoro-5-cyanouridine | A. A. Van Aerschot; D. H. Everaert; O. M. Peeters; N. M. Blaton; C. J. De Ranter; P. A. Herdewijn |
| 559-568 | Synthesis of (R - and (S)-1-[[2-Hydroxy-1-(aminomethyl)ethoxy]methyl]-5- benzyluracil, Potent Inhibitors of Uridine Phosphorylase | Tai-Shun Lin; Shi-Ping Xu; Mao-Chin Liu; William R. Mancini |
| 569-577 | The Enzymatic Synthesis of Imidazole Deoxynucleosides: 1-β-D-2′-Deoxyribofuranosyl-5-aminoiinidazole-4-carboxamide and 1-β-D-2′-Deoxyribofuranosylbenzimidazole | Didier Betbeder; David W. Hutchinson |
| 579-585 | Synthesis of 9-[(Phosphonomethoxy)methyl]guanine and 9-[2-Hydroxy-1-(phosphonomethoxy)ethyl]guanine | Choung Un Kim; Peter F. Misco; John C. Martin |
| 587-597 | Synthesis and Biological Activities of 3′-Deoxy-3′-Isocyano, -Isothiocyano, and -Isoselenocyano-thymidines | Akira Matsuda; Mutsumi Satoh; Tohru Ueda; Haruhiko Machida; Takuma Sasaki |
| 599-618 | Synthesis, Conformation and Hydrolytic Stability of p1,p3-Dinucleoside Triphosphates Related to mRNA 5′-cap, and Comparative Kinetic Studies on their Nucleoside and Nucleoside Monophosphate Analogs | Edward Darzynkiewicz; Janusz Stepinski; Stanley M. Tahara; Ryszard Stolarski; Irena Ekiel; Dorota Haber; Kari Neuvonen; Pertti Lehikoinen; Imre Labadi; Harri Lönnberg |
| 619-627 | 5′-C-Chain-Extended Adenosine Derivatives Related to Sinefungin. Synthesis and Biological Activity | John A. Secrist III; Ratnakar R. Talekar |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 8, Number 7 | |
| 1179-1188 | Nucleosides. 145. Synthesis of 2,5′-Anhydro-2-Thiouridine and its Conversion to 3′-O-Acetyl-2,2′-Anhydro-5′-Chloro-5′-Deoxy-2-Thiouridine. Studies Directed Toward the Synthesis of 2′-Deoxy-2′-Substituted arabino Nucleosides (7) | Ling-Ching Chen; Tsann-Long Su; Krzysztof W. Pankiewicz; Kyoichi A. Watanabe |
| 1189-1200 | Conformation and Antiherpes Activity of 3′- and 5′-Azido and Amino Analogs of 5-Methoxymethyl-2′-Deoxyuridine | Guy Tourigny; Allan L. Stuart; Irena Ekiel; Philip J. Aduma; Sagar V. Gupta |
| 1201-1216 | Synthesis of Tubercidin, 6-Chlorotubercidin and Related Nucleosides | Jack D. Anderson; Roger J. Bontems; Stewart Geary; Howard B. Cottam; Steven B. Larson; Steven S. Matsumoto; Donald F. Smee; Roland K. Robins |
| 1217-1229 | Evidence for the Stereoelectronic Control of the Acid Hydrolysis of Adenosine Cyclic 3′,5′-Phosphoramidate Diastereoisomers | S. Bottka; L. Radics; J. Tomasz |
| 1231-1257 | Synthesis and Biological Activity of the Mono- and Diamino Analogues of 2′-Deoxyadenosine, Cordycepin, 9-(3-Deoxy-α-D-Threo-Pentofuranosyl)-Adenine (A Structural Component of Agrocin 84) and 9-(2-Deoxy-α-D-Threo-Pentofuranosyl)Adenine | Piet Herdewijn; Jan Balzarini; Rudi Pauwels; Gerard Janssen; Arthur Van Aerschot; Erik De Clercq |
| 1259-1269 | Structural Features of 2′,3′-Dideoxy-2′,3′-Didehydrocytidine, A Potent Inhibitor of the HIV (AIDS) Virus | George I. Birnbaum; Jerzy Giziewicz; Tai-Shun Lin; William H. Prusoff |
| 1271-1280 | Ribosylation of 3-Methylguanine and the Relative Stability of its 7- and 9-α-D-Ribofuranosides | Jerzy Boryski; Tomasz Ostrowski; Bożenna Golankiewicz |
| 1281-1285 | An Unusual Iodine Monochloride Chlorination of an Imidazole Nucleoside | P. C. Srivastava; A. Hasan; R. Pratap; D. S. Bhakuni |
| 1287-1296 | An Unusual Reaction Observed in Sulfonylation and Acylation of 2′,3′-O-Isopropylidenenebularine | Hiroyuki Hayakawa; Hiroshi Ashizawa; Hiromichi Tanaka; Tadashi Miyasaka; Kentaro Yamaguchi |
| 1297-1303 | 31P-15N One-Bond Couplings of Diastereoisomeric Adenosine Cyclic 3′,5′-Phosphoramidates | J. Tomasz; S. Bottka; L. Radics |
| 1305-1317 | 9-(6-Deoxy- β -D-Allofuranosyl)Adenine Cyclic 3′,5′ -Phosphor-Amidate: A New Cyclic AMP Amide Derivative Containing an Equatorial Methyl Group at the 5′-Position | L. Radics; S. Bottka; J. Tomasz |
| 1319-1324 | Conversion of Methylthioadenosine Into its Naturally Occurring 3′-Isomer | Margherita Gavagnin; Guido Sodano |
| 1325-1334 | Synthesis of 5′-C-Chain-Extended Uridines by Reaction of 5′-Halonucleosides with Malonic Acid Type Derivatives | José Fiandor; María Teresa García-López; Federico G. De las Heras |
| 1335-1343 | Crystal and Molecular Structure of a Cytosine Analog; 5-Bromo-6-Benzylamino Isocytosine | Biswas Goutam; I. Iitaka; D. Shugar; Banerjee Asok |
| 1345-1358 | Nucleoside, XLV1) Synthese von 8-β-D-Ribofuranosyl-Leukopterin | Leonidas Kiriasis; Wolfgang Pfleiderer |
| 1359-1367 | Efficient Preparation of Cyclic 3′,5′-Phosphoramidites and -Amidates of Antiviral and Antitumor 5-X-2′-Deoxyuridines (X = H, CH3, I, F, CF3, trans-CH=CHBr) | Wesley G. Bentrude; Mamunur R. Khan; M. R. Saadein; Alan E. Sopchik |
| 1369-1377 | Synthesis of 2′-Deoxyformycin B and 2′-Deoxyoxoformycin B | Vishnu C. Solan; Andre Rosowsky |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 8, Number 5-6 | |
| 627-648 | Sugar-Modified Oligonucleotides: Synthesis, Physicochemical and Biological Properties | Jean-Louis Imbach; Bernard Rayner; François Morvan |
| 649-657 | Synthesis and Properties of Novel 5′-Linked Oligos | Kenya Mori; Chris Subasinghe; C. A. Stein; Jack S. Cohen |
| 659-671 | Anti-Hiv-1 Activity of 2′,3′-Dideoxinucleoside Analogues : Structure-Activity Relationship | Erik De Clercq; Arthur Van Aerschot; Piet Herdewijn; Masanori Baba; Rudi Pauwels; Jan Balzarini |
| 673-688 | Phosphonylalkoxyalkyl and Phosphonylalkyl Derivatives of Heterocyclic Bases | Antonln Holý; Ivan Rosenberg |
| 689-698 | Elucidation of the Mechanism by Which 9-(Trans-2′, Trans-3′-Dihydroxycyclopent-4′-enyl)-Adenine Lnactivates S-Adenosylhomocysteine Hydrolase and Elevates Cellular Levels of Sadenosylhomocysteinew | Steven D. Paisley; Masahide Hasobe; Ronald T. Borchardt |
| 699-708 | Development of Methodologies for the Strategic Modification of Purim Ribonwxeoside System | Vasu Nair |
| 709-724 | USE OF THE SODIUM SALT GLYCOSYLATION HETBOD IN NUCLEOSIDE SYNTHESIS | Ganapathi R. Revankar; Roland K. Robins |
| 725-741 | Synthesis, Transformation Chemistry, and Biological Activity of Guanine Nucleosides and Analoges | Moms J. Robins; Ruiming Zou; Fritz Hansske; Danuta Madej; David L. J. Tyrrell |
| 743-752 | SYNTHESIS AND BIOLOGICAL ACTIVITY OF BRANCHED CHAIN-SUGAR NUCLEOSIDES1 | Tohru Ueda; Akira Matsuda; Yuichi Yoshimura; Kenji Takenuki |
| 753-764 | New Potent and Selective Inhibitors of Herpes Simplex Virus Tbyhidine Kinase | J. A. Martin; I. B. Duncan; M. J. Hall; P. Wong-Kai-In; R. W. Lambert; G. J. Thomas |
| 765-774 | Membrane Transport of Nucleoside Analogues in Mammalian Cells | Thomas P. Zimmerman; Barbara A. Domin; William B. Mahony; Karen L. Prus |
| 775-785 | 2′,2′-Difluorodeoxycytidine Metabolism and Mechanism of Action In Human Leukemia Cells | William Plunkett; Varsha Gandi; Sherri Chubb; Billie Nowak; Volker Heinemann; Shin Mineishi; Alina Sen; Larry W. Herte; Gerald B. Grindey |
| 789-792 | Pyrazolo[3,4-d)Pyrimidine 2′-Deoxyribo and 2′,3′-Dideoxyribo-Furanosides: Synthesis and Application to Oligonucleotide Chemistry | F. Seela; H. Driller; K. Kaiser; H. Rosemeyer; H. Steker |
| 793-797 | Synthesis of Branched Oligoribonucleotides (“Lariat”) | N. Balgobin; X-X. Zhou; J-M. Vial; A. Nyilas; A. Földesi; J. Chattopadhyaya |
| 799-803 | The H-Phosphonate Method for Constructing Phosphodiester Linkages. A Progress Report | Jacek Stawiński; Roger Strömberg; Ingvar Lindh; Tor Regberg; Thomas Szabó; Mats Thelin; Erik Westman; Per J. Garegg |
| 805-813 | 5-Bromouridinylated Oligonucleotide for Hybridization Analysis of DNA and RNA on Membranes and in Situ | J. F. Ramalho Ortlgao; G. F. Jirikowski; H. Seliger |
| 815-818 | The Intracellular and Extracellular Fate of Oligodeoxyribonucleotides in Tissle Culture Systems | Marion Ceruzzi; Kenneth Draper |
| 819-823 | Phosphoramidate, Phosphorothioate, and Methylphosphonate Analogs of Oligodeoxynucleotide : Inhibitors of Replication of Human Immunodeficiency Virus | Sudhir Agrawal; John Goodchild; Maria Civeira; Prem S. Sarin; Paul C. Zamecnik |
| 825-828 | Antiviral activity of antisense oligonucleotides linked to poly(L-lysine):targets on genomic RNA and/or mRNA of Vesicular Stomatitis Virus | Jean-Paul Leonetti; Genevieve Degols; Pierre Milhaud; Corinne Gagnor; Marc Lemaitre; Bernard Lebleu |
| 829-832 | Acycloadenosine Derivatives as Inhibitors of 5′-Deoxy-5′-Methylthioadenosine Phosphorylase (MesADo PASE) | Shih-Hsi Chu; Zhi-Hao Chen; Todd M. Savarese; Charles E. Nakamura; Robert E. Parks Jr.; Elie Abushamb |
| 833-836 | EFFECT OF PHOSPHONIC ACID ANALOGS OF ACYCLOVIR AND GANCICLOVIR ON IN VITRO CYTOMEGALOVIRUS INFECTIONS | Robert W. Sidwell; John H. Huffman; Dale L. Barnard; Elmer J. Reist |
| 837-840 | Synthesis and Evaluation of Antiviral Activity of 3′-C-Cyano-3′-Deoxynucleosides | María-José Camarasa; Angel Díaz-Ortíz; Ana Calvo-hateo; Pederico G. De las Heras; Jan Balzarini; Erik de Clercq |
| 841-844 | Synthesis, Anti-Hiv Activity, and Biological Properties of 2′,3′-Didehydro-2′,3′-Dideoxythwidine (d4T) | John C. Martin; Muzammia M. Mansuri; John E. Starrett Jr.; Jean-Pierre Sommadossi; Vera Brankovan; Ismail Ghazzouli; H-T. Ho; Michael J. M. Hitchcock |
| 845-848 | Pharmacokinetics of A New Anti-HIV Ageht: 2′,3′-Dideoxy-2′,3′-Didehydrothymidine (d4T) | J. W. Russell; V. J. Whiterock; D. Marrero; L. J. Klunk |
| 849-853 | Synthesis and Biological Applications of 2′,3′-Dideoxynucleoside-5′-O-(α-thio)Triphosphates | M. Auer; C. Kriege; M. Gautel; S. Labeit; G. Sczakie; S. Weisz; R. S. Goody |
| 855-858 | Synthesis and Biological Properties of ( ) and (-)-(E)-5-(2-bronovinyl)-21 -deoxy-11 a-Carbauridine | Jan Balzarini; Harald Baumgartner; Michael Bodenteich; Erik De Clercq; Herfried Griengl |
| 859-862 | Synthesis of Novel Polycyclic Nucleoside Analogs | Norbert Bischofberger; Mark D. Matteucci |
| 863-866 | Apurinic DNA: Modelisation and Reactivity Towards 9-Aminoellipticine and Related Amines | Jean-Jacques Vasseur; Bernard Rayner; Jean-Louis Imbach; Jean-Remi Bertrand; Claude Malvy; Claude Paoletti |
| 867-870 | Regiocontrolled General Synthesis of Branch-Type 2′-5′-Linked Oligoadenylates | Y. Hayakawa; M. Hirose; R. Noyori |
| 871-874 | Base Analogues Related to N4-Hydroxicytosine | Paul V. S. Kong; Thoo Lin; D. M. Rrown |
| 875-877 | The Synthesis of Branched Oligonucleotides as Signal Amplification Multimers for Use in Nucleic Acid Assays | Thomas Horn; Brian D. Warner; Joyce A. Running; Kristi Downing; Jennifer Clyne; Mickey S. Urdea |
| 879-883 | Site-Specific 13C Labeling of DNA to Deduce DNA Repair Mechanisms of Uracil-DNA Glycosyiase and UV Endonuclease V | M. Manoharan; S. C. Ransom; A. Mazumder; J. A. Gerlt |
| 885-886 | Synthesis of Glycofuranosyl - formamides, -isocyanides and - isocyanates - Useful synthons for new approaches to nucleosid analogues | Johann Hebl; Johann Polsterer; Erich Zbiral |
| 887-890 | Synteesis of Certain C-4 Substituted Pyrazolo[3,4-b]-Pyridine Nucleosides Structurally Related to Adenosine and Inosine by Tee Sodiw Salt Glycosylation Procedure | Yogesh S. Sanghvi; Steven B. Larson; Roland K. Robins; Ganapathi R. Revankar |
| 891-894 | Synthesis and Biological Evaluation of 2-Carbamoyl-5-D-Ribofuranosylpyridine | F. C. Alderweireldt; I. Vrijens; E. L. Esmans; L. L. Wotring; L. B. Townsend; J. Balzarini; E. De Clercq |
| 895-898 | Sulfur Isosteres of Orotidine | Subhasish Purkayastha; Gabriel Menichi; Raymond P. Panzica |
| 899-902 | Novel Acyclic Derivatives of Aica-Riboside (1-(β-D-Ribopuranosyl)5-Amino-4-Imidazolecarboxamide), Potential Antiviral Agents | Thomas I. Kalman; D. Michael Houston |
| 903-906 | A General Synthetic Method for 2′,3′-Dideoxynucleosldes: Total Synthetic Approach | Chung K. Chu; Ramesh Raghavachari; J. Warren Beach; Yoshiyuki Kosugi; Giliyar V. Ullas |
| 907-910 | Unsaturated Nucleoside Analogues: Synthesis and Antitumor Activity | Shashikant Phadtare; David Kessel; Jiri Zemlicka |
| 911-913 | 8-Substituted Purine Ribosides: Synthesis and Biological Activity | Anita T. Shortnacy; John A. Montgomery; John A. Secriist III |
| 915-917 | Synthesis and Antiviral Evaluation of Adenosine-N1-Oxide and 1-(Benzyloxy) Adenosines | Charles A. Krauth; Anita T. Shortnacy; John K. Montgomery; John A. Secrist III |
| 919-922 | Synthesis of Phosphonic Acid Analogs of Acyclovir (ACV) and Canciclovir (DHPG) | Elmer J. Reist; Priscilla A. Sturm; Ronald Y. Pong; Robert W. Sidwell |
| 923-926 | Synthesis and Antiherpesvirus Activity of (S)-1-((3-Hydroxy-2-Phosphon-Ylmethoxy)Propyi.)Cytosine (HPMPC) and Related Nucleotide Analogues | John C. Martin; Joanne J. Bronson; Robert R. Webb II; Michael M. J. Hitchcock; Ismail Ghazzouli |
| 927-931 | Synthesis and Biological Activities of Phosphonylalkylpurine Derivatives | Choung Un Kim; Bing Yu Luh; Peter F. Misco; Joanne J. Bronson; Michael J. M. Hitchcock; Ismail Ghazzouli; John C. Martin |
| 933-937 | Some Examples of the Use of Trifluoromethane Sulfonic Anhydride in Nucleic Acid Chemistry | P. Herdewijn; A. Van Aerschot |
| 939-941 | Isomerization of Cytidine 2′,3′-Thionocarbonates | L. W. Dudycz |
| 943-946 | Synthesis of Some 2-Alkylated-5-Aminoimidazoles Related to Intermediates in Purine Nucleotide de novo and Thiamine Biosynthesis | Grahame Mackenzie; Hilary A. Wilson; Robert W. Humble; Fawzy Hewedi; Gordon Shaw; David Ewing |
| 947-950 | The Synthesis of 1-[7,8-Anhydr0-2,5,6-trideoxy-β-D-allo (and α-L-Talo)-Octofuranosyl]-Thymine as a Potential Enzyme Inhibitor | H. Jeanette Thomas; James M. Riordan; Robert D. Elliott; John A. Montgomery |
| 951-955 | Synthesis, Cytotoxicity and Metabolism of the 2′,2′-Difluoro-Analogs of Deoxyadenosine (dFdA)and Deoxyguanosine (dFdG) | L. W. Hertel; C. S. Grossmana; J. S. Kroina; S. Mineishi; S. Chubb; B. Nowak; W. Plunkett |
| 957-960 | An Unusual Dephosphorylation Reaction | Anne F. Cichy; Purushotham Vemishetti; Elie Abushanab |
| 961-965 | Syntiiesis of New 3′-Amino-2′,3′-Dideoxynucleosides in Five Steps Starting from Peracetylated Clycals | Jesper Lau; Erik B. Pedersen; Jesper Wengel |
| 967-968 | Synthesis of Anti-Sense Phosphorothioate Analogues for Pharmacokinetic and Pre-Clinical Studies | Alex Andrus; Timothy Geiser; Gerald Zon |
| 969-973 | Renal Deoxyadenosine Transport and Immunodeficiency Associated with Adenosine Deaminase Deficiency | J. Arly Nelson |
| 975-978 | Control of Differentiation by GTP | Ernst Freese |
| 979-982 | Enzymatic Synthesis of Radioactive 5-Methyl-2′-Deoxycytidine 5′-Monophosphate by Using 32P-Postlabeling | Juhani A. Vilpo; Leena M. Vilpo |
| 983-986 | Biosynthesis of the Naturally Occurring Nucleoside Antibiotics from Adenosine | Robert J. Suhadolnik; Jeffery C. Hanvey; Somchai Pornbanlualap; Joseph M. Wu; Kamal N. Tiwari; Anna K. Hebbler; David C. Baker |
| 987-990 | Phosphorothioate Analogs OF 2-5A: Activation / Inhibition of Rnase L and Inhibition of HIV-1 Reverse Transcriftase | Robert J. Suhadolnik; Bernard Lebleu; Wolfgang Pfleiderer; Ramamurthy Charubala; David C. Montefiori; William M. Mitchell; Robert W. Sobol Jr.; Shi Wu Li; Katalin Kariko; Nancy L. Reichenbach |
| 991-994 | Design and Chemoenzymatic Synthesis of A Tissue Plasminogen Activator Gene with Unique Restriction Sites: A Model for Studying Protein Domain Function | N. Theriault Hatzenbuhler; E. F. Rehberg; J. B. Carter; D. P. Palermo; E. V. Hubert; P. W. Bergum; L. A. Erickson; K. R. Marotti |
| 995-1000 | Alpba-Oligodeoxynucleotides as Inhibitors of HIV Reverse Transcriptase | R. Pauwels; Z. Debyser; J. Balzarini; M. Baba; J. Desmyter; B. Rayner; F. Morvan; J. L. Imbach; E. De Clercq |
| 1001-1006 | New Results in Oligoribonucleotide Synthesis | Magdalena Pfister; Wolfgang Pfleiderer |
| 1007-1010 | Stereochemical Problems in Oligonucleotide Synthesis | R. Charubala; K. P. Stengele; W. Pfleiderer |
| 1011-1014 | Synthesis of Oligodeoxynlicleotides Containing Specific Methylphosphonothioate and Dithioate Moieties | W. K. -D. Brill; M. H. Caruthers |
| 1015-1018 | Synthesis of Oligonucleotides Containing 5,6-Dihydro-5-Azacytosine and 5-Azacytosine at Specific CpG Sites | Amanda J. Goddard; Victor E. Marquez |
| 1019-1022 | General Synthesis of 2′(3′)-O-Aminoacyl Oligoribonucleotides Related to the 3′-Terminus of aa-tRNA | Michael D. Hagen; Stanislav Chlàdek |
| 1023-1027 | Synthetic Approaches to Oligodeoxyribonucleoside Phosphorodithioates Using Tervalent Phosphorus Monomers | Bjarne H. Dahl; Kirsten Bjergårde; Vibeke B. Sommer; Otto Dahl |
| 1029-1032 | Recent Studies in Nucleoside Phosphonate Chemistry | Jacek Stawinski; Roger Strömberg; Tomas Szabó; Erik Westman |
| 1033-1036 | Use of New Phosphonylating and Condensing Agents in The Synthesis of Oligonucleotides Via The H-Phosphonate Approach | Osamu Sakatsume; Hiroshi Yamane; Hiroshi Takaku |
| 1039-1040 | Inhibition of Purine Nucleoside Phosphorylase by Phosphonoalkylpurines 1 | Charles E. Nakamura; Shih-Hsi Chu; Johanna D. Stoeckler; Robert E. Parks Jr. |
| 1041-1042 | Rapid Synthesis of 2′ and 3′ Fluorinated Nucleotides and Their Use in 19F-NMR-Spectroscopy of Nucleotide-Binding Enzymes | M. Auer; P. Röisch; G. Sczakiel; R. S. Goody |
| 1043-1044 | 2 and 8-Azido ATP: Photoaffinity Labeling of 2-5A Synthetase, Enzymatic Synthesis of 2 and 8-Azido Anamgs of 2-5A for Use as Photoaffinity Probes of Rnase L | Shi Wu Li; Robert W. Sobol Jr.; Nancy L. Reichenbach; Katalin Kariko; Boyd E. Haley; Robert J. Suhadolnik |
| 1045-1046 | Use of A Uridine Nucleotide as an Affinity Handle and 5′ Phosphorylating Agent for Synthetic DNA | E. Higgins; J. S. Debear; P. C. Andrews; G. R. Gough |
| 1047-1048 | Large Scale HPLC Purification of Oligodeoxyribonucleotides for Studies of the Binding of CC-1065 to DNA by NMR Spectroscopy | S. P. Pulaski; N. Theriault Hatzenbuhler; T. A. Scahill; N. Richter |
| 1049-1050 | Sequence Preference of Acridine Interaction with Single and Double Stranded Octadeoxyribonucleotides | I. Lassalle; P. A. Hoyos; S. R. Byrn; H. L. Weith |
| 1051 | The Incorporation of 2,6-Diaminopurine Into Oligodeoxyribonucleotides by the Phosphoramidite Method | Tom Brown; Alister G. Craig |
| 1053-1054 | The Synthesis of αβ Imidothymidine Diphospate | Lawrence C. Davies |
| 1055-1056 | A Solid-Phase Synthesis of 2′,5′-Linked Oligoadenylates (2-5A) | Krystyna Lesiak; Bogdan Uznanski; Paul F. Terrence |
| 1057-1059 | Synthesis of (Dicarbonyl)(η5-cyclopentadieny1)iron -Derived Nucleoside Phosphonate Esters | Don Bergstrom; Theresa Schmaltz |
| 1061-1063 | Synthesis of (Dicarbonyl)(η5-cyclopentadienyl)Manganese Complex Stabilized Nucleoside Phosphite Esters | Don Bergstrom; Peter; Robert Lind |
| 1065-1068 | Deprotecton Studies of Ethanoic Acid 5,6,7,9-Tetrahydro-3-/2-(Acetoxyemxy Iethyl-5-0-Acetyl-9-OXO-3H-IMIDAZO/1,2a/ Purine-6,7-Dioyol Ester (1) and Related Glyoxal-Guaniee Adduts | J. Plavec; A. Štimac; A. Šmidovnik; J. Kobe |
| 1069-1070 | 2,3-Dideoxy-3-Phthalimidopentoses in the Synthesis of 3′-Amino-2′,3′-Dideoxynucleosides | Erik B. Pedersen; Mohammed S. Motawia; Erik S. Andreassen; Jesper Wengel; Jesper Lau |
| 1071-1072 | Photochemistry of the O-Nitrobenzyl Protecting Group in RNA Synthesis | J. A. Hayes; G. R. Gough; P. T. Gilham |
| 1073-1074 | C-5 Substituted Pyrimidine Nucleosides, Synthesis of 5-Alkylglycoside Deoxyuridine and Uridine Analogs VIA Organopalladium Intermediates | Sylvie Pochet; Simon R. Satfati; Jean Igolen |
| 1075-1076 | Synthesis of 2′ -Deoxypyrihidine Nucleosides Via Copper (I) Iodide Catalysis | John N. Freskos |
| 1077-1078 | The Role of Molecular Oxygen in the Catalytic Hydrogenation of Hydrazinonucleosides to the Corresponding Aminonucleosides | Vaidyanathan K. Iyer |
| 1079-1080 | The Synthesis of Pyrazol0[3,4-c]Pyridine C-Nucleosides | Daryl R. Sauer; Stewart W. Schneller |
| 1081-1082 | The Synthesis of the Carbocyclic Derivative of lin-Benzo-Separated 2′,3′-Dideoxyinosine | James W. Leahy; Stewart W. Schneller |
| 1083-1084 | A Convenient Synthesis of 9-(5′-DEOXY-β-D-Allofuranosyl)-Adenine (5′-Homoadenosine) | Ellen M. Salcines; Stewart W. Schneller |
| 1085-1086 | The Synthesis of Derivatives of 2-Arylamino ara-Carbocyclic Purine Nucleosides as Potential Anti-Viral Agents | Masakazu Koga; Stewart W. Schneller |
| 1087-1088 | Synthesis Of Pyrrolo[2,3-b]Pyridine Nucleosides by Solid-Liquid Phase-Transfer Clycosylation and Deoxycenation of 4-Chloropyrrolo[2,3-d]Pyrimidine 2′-Deoxyribofuranosides | F. Seela; R. Cumbiowski; H. -P. Muth; W. Bourgeois |
| 1089-1090 | Synthesis of Pyrrolo[3,2-C]Pyridine 2′-Deoxy-D-Ribo-, 2′,3′-Dideoxy-D-Ribo-, and D-Arabinofuranosyl Nucleosides | F. Seela; W. Bourgeois; T. Jürgens |
| 1091-1092 | Unambiguous Assignment of Anomeric Configuration of Nucleosides by Noe-Difference Spectroscopy | Cábor Tóth; Helmut Rosemeyer; Frank Seela |
| 1093-1095 | Novel Acyclic Analogues of 3′-Azido-3′ Deoxythymidine 1-Hydroxy-3-Azido-2-Propoxymethyl Derivatives | H. B. Lazrek; M. Taourirte; J. -L. Barascut; J. -L. Imbach |
| 1097-1100 | Synthesis of Acyclic Nucleoside Using Potassium Iodide as Catalyst | H. B. Lazrek; N. Redwane; J. -L. Barascut; J. -L. Imbach |
| 1101-1102 | Investigation of the Synthesis of 2-Carbamoylmethyl-6-D-Ribofuranosylpyridine | E. De Vos; E. L. Esmans; F. C. Alderweireldt; J. A. Lepoivre |
| 1103-1105 | Progress in the Synthesis of A Potential PNP Transition State Inhibitor | Robert D. Elliott; Shri Niwas; John A. Montgomery; John A. Secrist III |
| 1107-1108 | Synthesis of 3′-C-Substituted-2′,3′-Dideoxynucleosldes as Potential Antcaids Agents | J. Fiandor; D. M. Huryn; B. Sluboski; L. J. Todaro; S. Tam |
| 1109-1110 | Synthesis and Evaluation of 2′,3′-Dideoxy-9-Deazaadenoslne and Some Related Derivatives | S. Tam; M. Holman; R. S. Klein; M. Mitsuya; S. Broder |
| 1111-1114 | Synthesis and Biological Evaluation of Dideoxunucleosides Containing A Difluoromethylene Unit | Esa T. Jarvi; Prasad S. Sunkara; Terry L. Bowlin |
| 1115-1117 | 1-(2,3-Dideoxy-3-Fluoro-β-D-Ribofuranosyl)Tine (FDDT). Improved Preparation and Evaluation as a Potential Anti-Aids Agent | R. Sterzycki; M. Mansuri; V. Brankovan; R. Buroker; I. Ghazzouli; M. Hitchcock; J-P. Somrnadossi; J. C. Martin |
| 1119-1120 | Phosphate Modified Analogues of 5′-O-Phosphorylated 2′,3′-Dideoxynucleosides: Synthesis and Anti-HIV Activity | Robert M. Rigs; Robert N. Comber; John A. Montgomery; John A. Secrist III; Janet M. Leeds; Sara Chaffee; Michael S. Hershfield |
| 1121-1122 | Influence of Fluorination of the Sugar Moiety on the Anti-HIV-1 Activity of 2′,3′-Dideoxynucleosides | Arthur Van Aerschot; Jan Balzarini; Rudi Pauwels; Luk Kerremans; Erik De Clercq; Piet Herdewijn |
| 1123-1124 | Synthesis of 3′-Fluoro-3′-Deoxyribonucleosides; Anti-HIV-1 and Cytostatic Properties | Arthur Van Aerschot; Jan Balzarini; Erik De Clercq; Piet Herdewijn |
| 1125-1126 | Sugar and Base-Modified 2′,3′-Dideoxynucleosides as Potential Anti-Aids Drugs | Arthur Van Aerschot; Jan Balzarini; Rudi Pauwels; Piet Wigerinck; Erik De Clercq; Piet Herdewijn |
| 1127-1128 | Carbovir: A Carbocyclic Nucleoside with Potent and Selective Activity Against Human Immunodeficiency Virus (HIV) in Vitro | Robert Vince; Mel Hua; Jay Brownell; George C. Lavelle; Jeanine Qualls; William M. Shannon |
| 1129-1130 | 6,6′-Bis-[1-(6-Deoxy-β-D-Galacopyranosyl) Uracil] - A Tunicaminyl Uracil Analogue : Synthesis and Preliminary Biological Evaluation | M. Ariatti |
| 1131-1133 | Cyclopentenyl Cytosine (CPE-C). A Carbocyclic Nucleoside with Antitumor and Antiviral Properties | John S. Driscoll; Victor E. Marquez; Jacqueline Plowman |
| 1135-1140 | Synthesis and Biological Activity of Various Selenenyl and Tellurenyl-Substituted Deoxyuridines and Deoxyuridylates | Ralph J. Cisneros; Louis A. Silks III; Jerome D. Odom; R. Bruce Dunlap |
| 1141-1142 | Synthesis and Biological Activity of Certain 4-Substituted Imidazo[4,5-d]Pyridazine Nucleosides | Kakarla Ramesh; Raymond P. Panzica |
| 1143-1144 | Synthesis and Biological Evaluation of 4-Amino-1-β-D-Ribofuranosylpyrrolo[3,2-c]Pyriding (3-Deazatubercidin) | P. Franchetti; G. Cristalli; M. Grifantini; E. Nasini; S. Vittori |
| 1145-1146 | Synthesis of O-Benzyl Derivatives of 2′-Deoxy-5-Trifluoromethyluridine for Antitumor Agents | Jun-Ichi Yamashita; Hiroshi Matsumoto; Kazuhiro Kobayashi; Kazuharu Noguchi; Mitsugi Yasumoto; Tohru Ueda |
| 1147-1151 | Comparative Efficacy of Nucleoside Analogues Against African Swine Fever Virus “in Vitro” | Alessandra Pani; M. Elena Marongiu; Paolo La Colla |
| 1153-1154 | Synthesis of 5′-Substituted Analogues of Carbocyclic 3-Deazaadenosine as Potential Antivirals | J. A. Secrist; R. M. Brash; R. J. Gray; R. N. Comber; J. A. Montgomery |
| 1155-1156 | The Synthesis and Preliminary Biological Evaluations of Selected Analogues of the Potent Broad-Spectrum Antiviral Agent Ganciclovir 1′,3′-Cyclic Monophosphate1 (2′-Nor-cGMP) | M. Maccoss; A. F. Wagner; C. L. Cantone; R. A. Strelitz; A. Chen; W. T. Ashton; J. Hannah; R. L. Tolman; R. Bostedor; J. Germershausen; J. D. Karkas; H. C. Perry; A. K. Field |
| 1157-1158 | A Potent, Selective, Non-Substrate Inhibitor of HSV-I Thymidine Kinase: (±)-9-[[(Z)-2-(Hydroxymethyl)Cyclohexyl]Methyl]Guanine and Related Compounds | W. T. Ashton; L. C. Meurer; R. L. Tolman; J. D. Karkas; R. Liou; H. C. Perryt; S. M. Czelusniak; R. J. Klein |
| 1159-1160 | In Vitro and in Vivo Phlebovirus Inhibition by Nucleosides Related to Ribavirin | John H. Huffman; Robert W. Sidwell; Roland K. Robins; Ganapathi R. Revankar; Dominique Y. Pifat |
| 1161-1163 | Synthesis and Use of New Digoxicenin- Meled Hucleotides in Non-Radioactive Labeling and Detection of Nucleic Acids | K. Mühlegger; H. -G. Batz; S. Böhm; H. V. D. Eltz; H. -J. Höltke; Ch. Kessler |
| 1165-1167 | A New Option in Solid Phase Synthesis of DNA-Fragments | S. Berner; G. Gröger; K. Mühlegger; H. Seliger |
| 1169-1173 | Queuine Content of Hematopoietic and Neuronal Tissues | W. R. Farkas; B. J. Lifsey; T. J. Siard |
| 1175-1176 | Synthesis of Reagents for Fluorescence-Tagging of DNA | George L. Trainor; Frank W. Hobbs; Anthony J. Cocuzza; Pat N. Confalone |
| 1177-1178 | 2-Deoxy-D-Ribofuranosylation of Ethyl 5-Aminoimidazole-4-Carboxylate by Biotransformation and Chemical Methods | David Ewing; Robert W. Humble; Antonin Holy; Grahame Mackenzie; Gordon Shaw; Ivan Votruba |
| a | Editorial board page for “Nucleosides & Nucleotides”, Volume 7, Number 1 | |
| 1-21 | Reaction of 5-Halocytosine Derivatives with Cysteine | Bimal C. Pal; Chandrakanta Ghosh; Satinder K. Sethi; Bruce E. Suttle; James A. McCloskey |
| 23-35 | Nucleoside H-Phosphonates. IX. Possible Side-Reactions During Hydrogen Phosphonate Diester Formation | Tor Regberg; Jacek Stawinski; Roger Ströberg |
| 37-43 | A Simple, Preparative Procedure for N3-Anisoyluridine and O6-Diphenylcarbamoylguanosine 2′-O-(Tetrahydropyran-2-YL) Derivatives via The Corresponding 3′,5′-Dibenzoates | Kazuo Kamaike; Yoshihiro Hasegawa; Yoshiharu Ishido |
| 45-60 | Structure and Conformation of 1-β-D-Ribofuranosylpyridin-4-One-3- Carboxamide, A Novel Nucleoside from Human Urine with a Rare Ribose Pucker | T. Srikrishnan; R. Parthasarathy; J. L. Alderfer; S. P. Dutta; G. B. Chheda |
| 61-73 | Synthesis, Molecular Cloning and Expression of Genes Coding for Atrial Natriuretic Factors from Rat and Human | Hans Sachse; Gerd Hagendorff; Klaus Dieter Preuβ; Hari S. Sharma; Karl Heinz Scheit |
| 75-90 | Silica Gel Functionalised with Different Spacers as Solid Support for Oligonucleotide Synthesis | Arthur Van Aerschot; Piet Herdewijn; Hubert Vanderhaeghe |
| 91-102 | Synthesis of 5-Benzyl and 5-Benzyloxybenzyl 2,2′-Anhydrouridines and Related Nucleoside Analogs as Inhibitors of Uridine Phosphorylase | Shih Hsi Chu; Zum Yao Weng; Zhi Hao Chen; Elizabeth C. Rowe; Edward Chu; Fardos N. M. Naguib; Mahmoud H. el Kouni; Sungman Cha; Ming Y. Chu |
| 103-115 | Probing the Thymidylate Synthase Active site with Bisubstrate Analog Inhibitors | Said M. M. Bayomi; Diana I. Brixner; Hassan Eisa; Arthur D. Broom; Takamori Ueda; Yung-Chi Cheng |
| 117-120 | An Improved Preparation of Rp and Sp N6, N6, O2′ - Tri-Benzoyl-Adenosine-3′, 5′-Cyclic Phosphoranilidates | Marcel K. Eberle; Leszek Brzechffa |
| 121-128 | Preparation of 8-Chloropurine Nucleosides Through the Reaction Between their C-8 Lithiated Species and p-Toluenesulfonyl Chloride | Hiroyuki Hayakawa; Hiromichi Tanaka; Kazuhiro Haraguchi; Masami Mayumi; Masako Nakajima; Takashi Sakamaki; Tadashi Miyasaka |
| a | Editorial board page for “Nucleosides, Nucleotides & Nucleic Acids”, Volume 6, Number 4 | |
| 663-678 | Synthesis and Biological Activity of C-Acyclic Nucleosides of Imidazo [1,5-a]-1,3,5-Triazines | Bozenna Golankiewicz; Joanna Zeidler; Erik De Clercq |
| 679-689 | The Large Scale Synthesis and Chromatographic and Spectral Properties of a Series of Alkylated Thymine and Uracil-Containing Nucleosides. O2-, 3- and O4-Alkylpyrimidine Derivatives | Roy Saffhill |
| 691-698 | Ribonucleoside Diphosphate Adducts with Elliptinium Acetate, an Antitumor Agent | T. B. Tam Ha; Jean Bernadou; Bernard Meunier |
| 699-736 | Partial Protection of Carbohydrate Derivatives. Part 23.1 Simple, Efficient Procedure for the Preparation of 3′- and 2′-0-(Tetrahydropyran-2-YL)Ribonucleoside Derivatives Involving Highly Regioselective 2′,5′-DI-O-Acylation or that Followed by Acyl Migration on Silica Gel and Subsequent O-(Tetrahydropyran-2-YL)Ation | Kazuo Kamaike; Fumihiko Uemura; Shun-Ichi Yamakage; Shigeyoshi Nishino; Yoshiharu Ishido |
| 737-759 | Synthesis of Certain 4-Substituted-1-β-D-Ribofuranosyl-3-Hydroxypyrazoles Structurally Related to the Antibiotic Pyrazofurin | Yogesh S. Sanghvi; Krishna G. Upadhya; N. Kent Dalley; Roland K. Robins; Ganapathi R. Revankar |
| 761-774 | Synthesis of 2′,3′-Dideoxyribavirin | Yogesh S. Sanghvi; Naeem B. Hanna; Steven B. Larson; Roland K. Robins; Ganapathi R. Revankar |
| 775-783 | Conformations of Acyclonucleosides: Crystal Structure of 9-(4-Hydroxybutyl)Guanine, an Analogue of Acyclovir | George I. Birnbaum; Nils Gunnar Johansson; David Shugar |
| 785-792 | A 31P NMR Study of the Reaction of Adenosine 3′ 5′-Cyclic Monophosphate with 2, 4, 6-Triisopropylbenzenesulfonyl Chloride | J. Tomasz; S. Bottka; I. Pelozer |
| 793-802 | Synthesis and Biological Evaluation of some Acyclic Nucleoside Cyclic Phosphoramidate Derivatives | Hiroshi Takaku; Tsunehiko Ito; Shiro Yoshida; Tomoni Aoki; Erik De Clercq |
| 803-814 | Synthesis of Oligonucleotides Containing the Abasic Site Model Compound 1,4-Anhydro-2-Deoxy-D-Ribitol | Ramon Eritja; Peter A. Walker; Sandra K. Randall; Myron F. Goodman; Bruce E. Kaplan |