Resolution of isopropylidene-glycerol benzoate by sequential enzymatic hydrolysis and preferential crystallization
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference13 articles.
1. Tetrahedron report number 195 (R)- and (S)-2,3-0-isopropylideneglyceraldehyde in stereoselective organic synthesis
2. Mode of nucleophilic addition to epichlorohydrin and related species: chiral aryloxymethyloxiranes
3. Synthèse des (R)- et (S)-O-isopropylidène-1,2-glycérols. Détermination de la pureté optique
4. Total synthesis of (R)-glycerol acetonide and the antiepileptic and hypotensive drug (-)-.gamma.-amino-.beta.-hydroxybutyric acid (GABOB): use of vitamin C as a chiral starting material
5. The synthesis of Chiral Glycerides starting from D- and L-serine
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1. Biotransformations with Lipases;Biotechnology;2008-03-20
2. Temperature control of the enantioselectivity in the lipase-catalyzed resolutions;Future Directions in Biocatalysis;2007
3. Kinetic resolution of (R, S)-1,2-O-isopropylideneglycerol by esterification with dry mycelia of moulds;Journal of Molecular Catalysis B: Enzymatic;2006-08
4. Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters;Journal of Applied Microbiology;2005-10
5. Enhanced enantioselectivity of Bacillus coagulans in the hydrolysis of 1,2-O-isopropylidene glycerol esters by thermal knock-out of undesired enzymes;Tetrahedron: Asymmetry;2005-02
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