Unexpected enantioseparation of mandelic acids and their derivatives on 1,2,3-triazolo-linked quinine tert-butyl carbamate anion exchange-type chiral stationary phase-Reference-Cited by-同舟云学术

Unexpected enantioseparation of mandelic acids and their derivatives on 1,2,3-triazolo-linked quinine tert-butyl carbamate anion exchange-type chiral stationary phase

Published:2010-08-16 Issue:17-18 Volume:33 Page:2590-2598
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Science

Author:

Kacprzak Karol,Maier Norbert,Lindner Wolfgang

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Reference36 articles.

1. Separation of enantiomers: needs, challenges, perspectives

2. Stereoselective Chromatographic Methods for Drug Analysis

3. Chiral recognition by enantioselective liquid chromatography: Mechanisms and modern chiral stationary phases

4. Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein

5. Application and comparison of immobilized and coated amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phases for the enantioselective separation of β-blockers enantiomers by liquid chromatography

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3. Effect of the Concentration of an Organic Modifier in a Water–Ethanol Mobile Phase on the Retention and Thermodynamics of Adsorption of Enantiomers of Hydroxy Acids and Their Derivatives on a Chiral Adsorbent with a Grafted Antibiotic Eremomycin;Russian Journal of Physical Chemistry A;2019-06

4. Aqueous Biphasic Systems Using Chiral Ionic Liquids for the Enantioseparation of Mandelic Acid Enantiomers;Solvent Extraction and Ion Exchange;2018-09-19

5. Liquid chromatographic enantiomer separations applying chiral ion-exchangers based on Cinchona alkaloids;Journal of Pharmaceutical and Biomedical Analysis;2018-09