Zwitterionic chiral stationary phases based on cinchona and chiral sulfonic acids for the direct stereoselective separation of amino acids and other amphoteric compounds-Reference-Cited by-同舟云学术

Zwitterionic chiral stationary phases based on cinchona and chiral sulfonic acids for the direct stereoselective separation of amino acids and other amphoteric compounds

Published:2014-04-13 Issue:11 Volume:37 Page:1237-1247
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Science

Author:

Zhang Tong¹,Holder Emilie¹,Franco Pilar¹,Lindner Wolfgang²

Affiliation:

1. Chiral Technologies Europe; Bd. Gonthier d’Andernach; Illkirch France

2. Department of Analytical Chemistry; University of Vienna; Vienna Austria

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jssc.201400149/fullpdf

Reference33 articles.

1. Separation of enantiomers by gas liquid chromatography with an optically active stationary phase

2. Ligand chromatography as a novel method for the investigation of mixed complexes: stereoselective effects in α-amino acid copper(II) complexes

3. Enantiomeric separation of nonproteinogenic amino acids by high-performance liquid chromatography

4. Chromatographic separation of racemic amino acids by use of chiral crown ether-coated reversed-phase packings

5. Preparation and application of a new ligand exchange chiral stationary phase for the liquid chromatographic resolution of α-amino acid enantiomers

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