Enhanced enantioselectivity of Bacillus coagulans in the hydrolysis of 1,2-O-isopropylidene glycerol esters by thermal knock-out of undesired enzymes-Reference-Cited by-同舟云学术

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Enhanced enantioselectivity of Bacillus coagulans in the hydrolysis of 1,2-O-isopropylidene glycerol esters by thermal knock-out of undesired enzymes

Published:2005-02 Issue:4 Volume:16 Page:841-845
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Romano Diego,Falcioni Francesco,Mora Diego,Molinari Francesco,Buthe Andreas,Ansorge-Schumacher Marion

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference12 articles.

1. Tetrahedron report number 195 (R)- and (S)-2,3-0-isopropylideneglyceraldehyde in stereoselective organic synthesis

2. The efficient synthesis of mixed diacyl phospholipids with polyunsaturated fatty acid in sn-2 position of glycerol

3. Enzymatic resolution of 2,2-disubstituted-1,3-dioxolane-4-methanol carboxylic esters

4. Lipase-catalyzed synthesis of monostearoylglycerol in organic solvents from 1,2-O-isopropylidene glycerol

5. Resolution of isopropylidene-glycerol benzoate by sequential enzymatic hydrolysis and preferential crystallization

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