Chiral Recognition of Peptide Enantiomers by Cinchona Alkaloid Derived Chiral Selectors: Mechanistic Investigations by Liquid Chromatography, NMR Spectroscopy, and Molecular Modeling-Reference-Cited by-同舟云学术

Chiral Recognition of Peptide Enantiomers by Cinchona Alkaloid Derived Chiral Selectors: Mechanistic Investigations by Liquid Chromatography, NMR Spectroscopy, and Molecular Modeling

Published:2003-10-01 Issue:22 Volume:68 Page:8315-8327
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Czerwenka Christoph¹,Zhang Mei Mei¹,Kählig Hanspeter¹,Maier Norbert M.¹,Lipkowitz Kenny B.¹,Lindner Wolfgang¹

Affiliation:

1. Institute of Analytical Chemistry, University of Vienna, Währingerstrasse 38, 1090 Wien, Austria, Department of Chemistry, North Dakota State University, Fargo, North Dakota 58105, and Institute of Organic Chemistry, University of Vienna, Währingerstrasse 38, 1090 Wien, Austria

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0346914

Reference35 articles.

1. Separation of enantiomers: needs, challenges, perspectives

2. Quinine and quinidine derivatives as chiral selectors I. Brush type chiral stationary phases for high-performance liquid chromatography based on cinchonan carbamates and their application as chiral anion exchangers

3. Enantioselective anion exchangers based on cinchona alkaloid-derived carbamates: Influence of C8/C9 stereochemistry on chiral recognition

4. Quinine- versus carbamoylated quinine-based chiral anion exchangers

5. Direct High-Performance Liquid Chromatographic Separation of Peptide Enantiomers: Study on Chiral Recognition by Systematic Evaluation of the Influence of Structural Features of the Chiral Selectors on Enantioselectivity

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