Diastereomeric and enantiomeric separation of monoesters prepared from meso-cyclopentanediols and racemic carboxylic acids on a silica phase and on amylose and cellulose chiral stationary phases-Reference-Cited by-同舟云学术

Diastereomeric and enantiomeric separation of monoesters prepared from meso-cyclopentanediols and racemic carboxylic acids on a silica phase and on amylose and cellulose chiral stationary phases

Published:1994-10 Issue:1 Volume:684 Page:162-167
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Kunath Annamarie,Theil Fritz,Wagner Jürgen

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference8 articles.

1. “Double enantioselection” by a lipase-catalyzed transesterification of a meso-Diol with a racemic carboxylic ester

2. Double enantioselective transesterification of racemic carboxylic esters and cyclic meso-diols by lipase catalysis

3. Instruction Manual for Chiracel OD, Daicel Chemical Industries, Tokyo.

4. Chromatographic resolution

5. Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phases

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