Analysis of the Mechanism of Retention on a Modified β‐Cyclodextrin/Silica Chiral Stationary Phase using a Computational Chemical Method
Author:
Affiliation:
1. a Laboratoire d'Analyse Organique Fonctionnelle, U.S.T.H.B., Faculté de Chimie , Alger, Algeria
2. b Health Research Foundation, Institut Pasteur , Kyoto, Japan
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10826070701632345
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4. Computational chemical analysis of chiral recognition in liquid chromatography, selectivity of N-(R)-1-(α-naphthyl)ethylamino carbonyl-(R or S)-valine and N-(S)-1-(α-naphthyl)ethylamino carbonyl-(R or S)-valine bonded aminopropyl silica gels
5. Computational Chemical Analysis of the Separation of Derivatized R- and S-Amino Acid Enantiomers on N-(tert-Butylaminocarbonyl)-(S)-valylamino- propylsilica Gel and (R)-1-(α-Naphthyl)-ethylaminocarbonyl-glycylamino-propylsilica Gel by Liquid Chromatography
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1. Comparison of HPLC enantioseparation of substituted binaphthyls on CD-, polysaccharide- and synthetic polymer-based chiral stationary phases;Journal of Separation Science;2010-03-03
2. Quantitative In Silico Analysis of the Specificity of a Graphitic Carbon Column;Journal of Liquid Chromatography & Related Technologies;2009-01-28
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