Influence of the nature of alkyl substituents on the high-performance liquid chromatography enantioseparation and retention of new atropisomeric 1,1′-bibenzimidazole derivatives on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase-Reference-Cited by-同舟云学术

Influence of the nature of alkyl substituents on the high-performance liquid chromatography enantioseparation and retention of new atropisomeric 1,1′-bibenzimidazole derivatives on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase

Published:2014-10 Issue: Volume:1363 Page:128-136
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Rizzo Simona,Menta Sergio,Faggi Cristina,Pierini Marco,Cirilli Roberto

Funder

Fondazione Cariplo

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference27 articles.

1. Polysaccharide Derivatives for Chromatographic Separation of Enantiomers

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

3. Solvent versatility of immobilized 3,5-dimethylphenylcarbamate of amylose in enantiomeric separations by HPLC

4. Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers

5. Enantioseparation of selected chiral sulfoxides using polysaccharide-type chiral stationary phases and polar organic, polar aqueous–organic and normal-phase eluents

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