Impact of the degree of substitution on the enantioseparation of anionic β-cyclodextrin in liquid‒liquid extraction and countercurrent chromatography: Insights from molecular docking simulations-Reference-Cited by-同舟云学术

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Impact of the degree of substitution on the enantioseparation of anionic β-cyclodextrin in liquid‒liquid extraction and countercurrent chromatography: Insights from molecular docking simulations

Published:2024-09 Issue: Volume:1733 Page:465255
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Sun Wenyu,Qiu Huiyun,Lin Susu,Tong Shengqiang^ORCID

Funder

National Natural Science Foundation of China-Yunnan Joint Fund

Project for Key Medicine Discipline Construction of Guangzhou Municipality

National Aerospace Science Foundation of China

Publisher

Elsevier BV

Reference39 articles.

1. Cyclodextrin rotaxanes and polyrotaxanes;Wenz;Chem. Rev.,2006

2. Experimental characterization of the association of beta-cyclodextrin and eight novel cyclodextrin derivatives with two guest compounds;Kellett;J. Comput. Aided Mol. Des.,2021

3. Cyclodextrin chiral stationary phases for liquid chromatographic separations of drug stereoisomers;Berthod;J. Pharm. Biomed. Anal.,1990

4. Cyclodextrin bonded phases for the liquid chromatographic separation of optical, geometrical, and structural isomers;Armstrong;J. Chromatogr. Sci.,1984

5. Cyclodextrins as chiral selectors in capillary electrophoresis: recent trends in mechanistic studies;Chankvetadze;Trac-Trend Anal Chem,2023

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