Chiral recognition ability of amylose derivatives bearing regioselectively different carbamate pendants at 2,3- and 6-positions-Reference-Cited by-同舟云学术

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Chiral recognition ability of amylose derivatives bearing regioselectively different carbamate pendants at 2,3- and 6-positions

Published:2019-08 Issue: Volume:218 Page:30-36
ISSN:0144-8617
Container-title:Carbohydrate Polymers
language:en
Short-container-title:Carbohydrate Polymers

Author:

Dai Xiao,Bi Wanying,Sun Mengchen,Wang Fan,Shen Jun^ORCID,Okamoto Yoshio

Funder

National Natural Science Foundation of China

Natural Science Foundation of Heilongjiang Province

Postdoctoral Science Foundation of Heilongjiang Province

Daicel Corporation (Tokyo, Japan)

Publisher

Elsevier BV

Subject

Materials Chemistry,Polymers and Plastics,Organic Chemistry

Reference33 articles.

1. A chromatographic study on the exceptional chiral recognition of 2-(benzylsulfinyl)benzamide by an immobilized-type chiral stationary phase based on cellulose tris(3,5-dichlorophenylcarbamate);Carradori;Journal of Chromatography A,2018

2. Comprehensive chirality, separations and analysis;Carreira,2012

3. Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers;Chankvetadze;Journal of Chromatography A,2012

4. 3-Fluoro-, 3-chloro-and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation;Chankvetadze;Journal of Chromatography A,1997

5. Chloromethylphenylcarbamate derivatives of cellulose as chiral stationary phases for high-performance liquid chromatography;Chankvetadze;Journal of Chromatography A,1994

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3. Regioselective modification at the 2,3- and 6-positions of chitosan with phenylcarbamates for chromatographic enantioseparation;Journal of Chromatography A;2024-01

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