Separation of enantiomers of chiral basic drugs with amylose- and cellulose- phenylcarbamate-based chiral columns in acetonitrile and aqueous-acetonitrile in high-performance liquid chromatography with a focus on substituent electron-donor and electron-acceptor effects-Reference-Cited by-同舟云学术

Separation of enantiomers of chiral basic drugs with amylose- and cellulose- phenylcarbamate-based chiral columns in acetonitrile and aqueous-acetonitrile in high-performance liquid chromatography with a focus on substituent electron-donor and electron-acceptor effects

Published:2020-08 Issue: Volume:1624 Page:461218
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Matarashvili Iza,Chelidze Aluda,Dolidze Gizo,Kobidze Giorgi,Zaqashvili Nino,Dadianidze Alexandre,Bacskay Ivett,Felinger Attila^ORCID,Farkas Tivadar,Chankvetadze Bezhan

Funder

NKFIH

OTKA

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference37 articles.

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2. Chromatographic resolution: XI. Controlled chiral recognition of cellulose triphenylcarbamate derivatives supported on silica gel;Okamoto;J. Chromatogr.,1986

3. Useful chiral stationary phases for HPLC. Amylose tris(3,5-dimethylphenylcarbamate) and tris(3,5-dichlorophenylcarbamate) supported on silica gel;Okamoto;Chem. Lett.,1987

4. Tris(chloro- and methyl-disubstituted phenylcarbamate)s of cellulose as chiral stationary phases for chromatographic enantioseparation;Chankvetadze;Chem. Lett.,1993

5. Chloro-methyl-phenylcarbamate derivatives of cellulose as chiral stationary phases for high performance liquid chromatography;Chankvetadze;J. Chromatogr. A.,1994

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