Enantiomer separation of some aromatic carboxylic acids by HPLC on a chemically bonded β-cyclodextrin stationary phase
Author:
Publisher
Wiley
Subject
General Chemical Engineering
Reference4 articles.
1. Retention behavior of some aromatic compounds on chemically bonded cyclodextrin silica stationary phase in liquid chromatography
2. Rapid method for packing microparticulate columns packed with a chemically bonded stationary phase for high-performance liquid chromatography
3. Enantiomeric resolution of 1-[2-(3-hydroxyphenyl)-1-phenylethyl]-4- (3-methyl-2-butenyl)piperazine by reversed-phase high-performance liquid chromatography using a chiral mobile phase
4. Resolution of some chiral mandelic acid derivatives into enantiomers by reversed-phase high-performance liquid chromatography via α- and β-cyclodextrin inclusion complexes
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1. Cyclodextrin-Based Chiral Stationary Phases;Chiral Separations By Liquid Chromatography And Related Technologies;2003-06-03
2. Synthesis and applications of adsorbents containing cyclodextrins;Journal of Separation Science;2002-09-01
3. Chromatographic separations of aromatic carboxylic acids;Journal of Chromatography B: Biomedical Sciences and Applications;1998-10
4. Chiral separation of pharmaceuticals possessing a carboxy moiety;Journal of Chromatography B: Biomedical Sciences and Applications;1998-10
5. Direct separation of carboxylic acid enantiomers by high-performance liquid chromatography with amide and urea derivatives bonded to silica gel as chiral stationary phases;Journal of Chromatography A;1995-01
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