Versatility of cinchona-based zwitterionic chiral stationary phases: Enantiomer and diastereomer separations of non-protected oligopeptides utilizing a multi-modal chiral recognition mechanism-Reference-Cited by-同舟云学术

Versatility of cinchona-based zwitterionic chiral stationary phases: Enantiomer and diastereomer separations of non-protected oligopeptides utilizing a multi-modal chiral recognition mechanism

Published:2012-12 Issue: Volume:1269 Page:297-307
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Wernisch Stefanie,Lindner Wolfgang

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference35 articles.

1. Chirality of Living Systems: A Helping Hand from Crystals and Oligopeptides

2. Homochirality and chemical evolution: new vistas and reflections on recent models

3. Polypeptide Chains Containing d-γ-Hydroxyvaline

4. Amino acid sequence andD/L-configuration determination methods forD-amino acid-containing peptides in living organisms

5. Computational Design of Thermostabilizing d-Amino Acid Substitutions

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3. Chiral Stationary Phases Derived from Cinchona Alkaloids;Chiral Separations and Stereochemical Elucidation;2023-03-26

4. Chiral separation of dipeptides on Cinchona‐based zwitterionic chiral stationary phases under buffer‐free reversed‐phase conditions;Chirality;2022-05-20

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