Structural factors affecting the enantiomeric separation of barbiturates and thiobarbiturates with a chiral side-chain by various β-cyclodextrin supports. Effects of the presence of hydroxypropyl substituents on the chiral selector-Reference-Cited by-同舟云学术

Structural factors affecting the enantiomeric separation of barbiturates and thiobarbiturates with a chiral side-chain by various β-cyclodextrin supports. Effects of the presence of hydroxypropyl substituents on the chiral selector

Published:1994-11 Issue:1 Volume:685 Page:15-20
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Thuaud N.,Sebille B.

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference15 articles.

1. D.W. Armstrong, U.S. Pat., 4 539 399 (1985).

2. Derivatized cyclodextrins for normal-phase liquid chromatographic separation of enantiomers

3. (S)-2-Hydroxyprophyl-β-cyclodextrin, a new chiral stationary phase for reversed-phase liquid chromatography

4. Retention behavior and chiral recognition of β-cyclodextrinderivative polymer adsorbed on silica for warfarin, structurally related compounds and Dns-amino acids

5. Enantiomer separations with chromatographic supports based on β-cyclodextrin polymers immobilized on porous silica. Role of the polymer structure in separating ability

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