Structure-enantioselectivity relationships for the study of chiral recognition in peptide enantiomer separation on cinchona alkaloid-based chiral stationary phases by HPLC: Influence of the N-terminal protecting group-Reference-Cited by-同舟云学术

Structure-enantioselectivity relationships for the study of chiral recognition in peptide enantiomer separation on cinchona alkaloid-based chiral stationary phases by HPLC: Influence of the N-terminal protecting group

Published:2003-11-01 Issue:17 Volume:26 Page:1499-1508
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Science

Author:

Czerwenka Christoph,Lämmerhofer Michael,Lindner Wolfgang

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Reference21 articles.

1. Chromatographic resolution of dipeptide enantiomers and diastereomers on chiral stationary phases from poly-(L-leucine) or poly(L-phenylalanine)

2. High Performance Liquid Chromatographic Enantioresolution of Benzoyl Amino Acid, Dipeptides and Tripeptide on β-Cyclodextrin Bonded Stationary Phase Using Polar-Organic Acetonitrile as the Mobile Phase

3. Micro-HPLC and standard-size HPLC for the separation of peptide stereoisomers employing an ion-exchange principle

4. Enantioseparation of amino acids and dipeptides using vancomycin as chiral selector in capillary electrophoresis

5. Chiral separation ofDL-peptides and enantioselective interactions between teicoplanin andD-peptides in capillary electrophoresis

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