Kinetic resolution of racemic β,γ-epoxy esters with pig liver esterase (PLE, e.c. 3.1.1.1.)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver Esterase
2. Enhanced and reversed enantioselectivity of enzymic hydrolysis by simple substrate modifications: the case of 3-hydroxyglutarate diesters
3. Synthesis of (S)- and (R)-4[(methoxycarbonyl)methyl]-2-azetidinone by chemicoenzymic approach
4. Enzymes in organic synthesis. 35. Stereoselective pig liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters. Optimization of enantiomeric excess via reaction conditions control
5. Enantioselective hydrolysis of dialkyl 3-monosubstituted glutarates with pig liver esterase: Structure-optical purity relationships
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