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Journal of Chromatography A
Copyright © 2001 Elsevier Science B.V. All rights reserved

Volume 694, Issue 1,
Pages 3-313 (3 March 1995)

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1.
Molecular imprinting used for chiral separations, Pages 3-13
Maria Kempe and Klaus Mosbach
Abstract | Journal Format-PDF (632 K)


2.
Theoretical studies of type II-V chiral stationary phases, Pages 15-37
Kenny B. Lipkowitz
Abstract | Journal Format-PDF (1481 K)

3.
Stereochemical determinants of the nature and consequences of drug metabolism, Pages 39-48
John Caldwell
Abstract | Journal Format-PDF (681 K)

4.
Influence of the method of preparation of chiral stationary phases on enantiomer separations in high-performance liquid chromatography, Pages 49-56
Toshihide Ihara, Yoshio Sugimoto, Makoto Asada, Tatsuro Nakagama and Toshiyuki Hobo
Abstract | Journal Format-PDF (437 K)

5.
Optimization of the separation of enantiomers of basic drugs Retention mechanisms and dynamic modification of the chiral bonding properties on an 1-acid glycoprotein column, Pages 57-69
Jörgen Hermansson and Anders Grahn
Abstract | Journal Format-PDF (601 K)

6.
Enantioselectivity of bovine serum albumin-bonded columns produced with isolated protein fragments, Pages 71-80
Jun Haginaka and Naoko Kanasugi
Abstract | Journal Format-PDF (487 K)

7.
Study of the enantioselective binding between BOF-4272 and serum albumins by means of high-performance frontal analysis, Pages 81-89
Akimasa Shibukawa, Miki Kadohara, He Jing-yi, Masuhiro Nishimura, Shinsaku Naito and Terumichi Nakagawa
Abstract | Journal Format-PDF (518 K)

8.
Development of chiral stationary phases consisting of polysaccharide derivatives, Pages 91-100
Kazuma Oguni, Hirofumi Oda and Akito Ichida
Abstract | Journal Format-PDF (445 K)

9.
Dimethyl-, dichloro- and chloromethylphenylcarbamates of amylose as chiral stationary phases for high-performance liquid chromatography, Pages 101-109
Bezhan Chankvetadze, Eiji Yashima and Yoshio Okamoto
Abstract | Journal Format-PDF (476 K)

10.
Preparation and chromatographic characteristics of a chiral-recognizing perphenylated cyclodextrin column, Pages 111-118
Kazuo Nakamura, Hiroya Fujima, Hiroshi Kitagawa, Hiroo Wada and Keisuke Makino
Abstract | Journal Format-PDF (366 K)

11.
Unified enantioselective capillary chromatography on a Chirasil-DEX stationary phase Advantages of column miniaturization, Pages 119-128
V. Schurig, M. Jung, S. Mayer, M. Fluck, S. Negura and H. Jakubetz
Abstract | Journal Format-PDF (500 K)

12.
Direct enantiomer separations by high-performance liquid chromatography with chiral urea derivatives as stationary phases, Pages 129-134
Naobumi Ôi, Hajimu Kitahara and Fumiko Aoki
Abstract | Journal Format-PDF (265 K)

13.
Comparison of (S)-N-(3,5-dinitrobenzoyl)tyrosine derivatives as chiral selectors for high-performance liquid chromatographic enantioseparations, Pages 135-150
E. Veigl, B. Böhs, A. Mandl, D. Krametter and W. Lindner
Abstract | Journal Format-PDF (599 K)

14.
Evaluation of silica gel-based brush type chiral cation exchangers with (S)-N-(3,5-dinitrobenzoyl)tyrosine as chiral selector: attempt to interpret the discouraging results, Pages 151-161
E. Veigl, B. Böhs, A. Mandl, D. Krametter and W. Lindner
Abstract | Journal Format-PDF (587 K)

15.
Behaviour of allyl aryl sulfoxides in high-performance liquid chromatography on a chiral stationary phase, Pages 163-167
F. Gasparrini, D. Misiti and C. Villani
Abstract | Journal Format-PDF (206 K)

16.
Using chirality as a unique probe of pharmacological properties, Pages 169-179
Irving W. Wainer, Julie Ducharme, Camille P. Granvil, Heli Parenteau and Sami Abdullah
Abstract | Journal Format-PDF (568 K)

17.
Stereoselective pharmacokinetics of dihydropyridine calcium antagonists, Pages 181-193
Yoji Tokuma and Hideyo Noguchi
Abstract | Journal Format-PDF (768 K)

18.
Diastereomeric -lactam antibiotics Analytical methods, isomerization and stereoselective pharmacokinetics, Pages 195-208
Tomoo Itoh and Hideo Yamada
Abstract | Journal Format-PDF (869 K)

19.
Direct determination of E2020 enantiomers in plasma by liquid chromatography-mass spectrometry and column-switching techniques, Pages 209-218
Kenji Matsui, Yoshiya Oda, Hiroshi Ohe, Shigeru Tanaka and Naoki Asakawa
Abstract | Journal Format-PDF (432 K)

20.
Investigation of the stereoselective metabolism of the chiral H1-antihistaminic drug terfenadine by high-performance liquid chromatography, Pages 219-225
A. Terhechte and G. Blaschke
Abstract | Journal Format-PDF (330 K)

21.
Gas chromatographic separation of enantiomeric amino acids and amines with -methoxy--trifluoromethylpropionic acid as a chiral derivatizing agent, Pages 227-236
Fujiko Yasuhara, Shozo Yamaguchi, Masayuki Takeda, Yoshiro Ochiai and Sotaro Miyano
Abstract | Journal Format-PDF (514 K)

22.
Gas chromatographic enantiomer separation of pharmaceuticals on capillary columns coated with novel chiral polysiloxanes, Pages 237-243
Iwao Abe, Takako Nishiyama, Taketoshi Nakahara and Hartmut Frank
Abstract | Journal Format-PDF (360 K)

23.
Optical resolution of drugs by capillary electrophoretic techniques, Pages 245-276
Hiroyuki Nishi and Shigeru Terabe
Abstract | Journal Format-PDF (1582 K)

24.
Partial separation zone technique for the separation of enantiomers by affinity electrokinetic chromatography with proteins as chiral pseudo-stationary phases, Pages 277-284
Yoshihide Tanaka and Shigeru Terabe
Abstract | Journal Format-PDF (493 K)

25.
Protein chiral selectors in free-solution capillary electrophoresis and packed-capillary electrochromatography, Pages 285-296
David K. Lloyd, Li Song and Patricia Ryan
Abstract | Journal Format-PDF (772 K)

26.
Use of cyclodextrins in capillary electrophoresis for the chiral resolution of some 2-arylpropionic acid non-steroidal anti-inflammatory drugs, Pages 297-305
Salvatore Fanali and Zeineb Aturki
Abstract | Journal Format-PDF (515 K)

27.
Ability of non-cyclic oligosaccharides to form molecular complexes and its use for chiral separation by capillary zone electrophoresis, Pages 307-313
Koji Kano, Kenji Minami, Kazumi Horiguchi, Taizo Ishimura and Masahito Kodera
Abstract | Journal Format-PDF (391 K)


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