High-Performance Liquid Chromatographic Enantioseparation of Cyclic β -Amino Acids on Zwitterionic Chiral Stationary Phases Based on Cinchona Alkaloids
Author:
Affiliation:
1. Department of Inorganic and Analytical Chemistry; University of Szeged; Szeged Hungary
2. Institute of Pharmaceutical Chemistry; University of Szeged; Szeged Hungary
3. Department of Analytical Chemistry; University of Vienna; Vienna Austria
Funder
Hungarian National Science Foundation
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chir.22458/fullpdf
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3. Diexo-3-aminonorbornane-2-carboxylic acid as highly applicable chiral source for the enantioselective synthesis of heterocycles;Fülöp;Synlett,2008
4. Synthesis of orthogonally protected azepane ß-amino ester enantiomers;Kazi;Tetrahedron Lett,2010
5. Application of alicyclic β-amino acids in peptide chemistry;Fülöp;Chem Soc Rev,2006
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1. Novel chiral stationary phases based on 3,5‐dimethyl phenylcarbamoylated β‐cyclodextrin combining cinchona alkaloid moiety;Chirality;2020-05-08
2. Cinchona-based zwitterionic stationary phases: Exploring retention and enantioseparation mechanisms in supercritical fluid chromatography with a fragmentation approach;Journal of Chromatography A;2020-02
3. Enantioselective resolution of biologically active dipeptide analogs by high-performance liquid chromatography applying Cinchona alkaloid-based ion-exchanger chiral stationary phases;Journal of Chromatography A;2020-01
4. Recent developments in liquid and supercritical fluid chromatographic enantioseparations;Handbook of Analytical Separations;2020
5. Cinchona Alkaloid-Based Zwitterionic Chiral Stationary Phases Applied for Liquid Chromatographic Enantiomer Separations: An Overview;Methods in Molecular Biology;2019
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