Differences in reactivity and enantioselectivity in lipase reactions with carboxylic esters and alcohols bearing the same stereogenic center
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference6 articles.
1. Synthesis of chiral building blocks for selective adenosine receptor agents. Lipase-catalyzed resolution of 2-benzylpropanol and 2-benzylpropionic acid.
2. Chemoenzymatic synthesis of the enantiomers of iopanoic acid
3. Quantitative analyses of biochemical kinetic resolutions of enantiomers
4. Enhancing the enantioselectivity of Candida lipase-catalyzed ester hydrolysis via noncovalent enzyme modification
5. Double enantioselective esterification of racemic acids and alcohols by lipase from Candida cylindracea
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2. Identification of an Esterase Isolated Using Metagenomic Technology which Displays an Unusual Substrate Scope and its Characterisation as an Enantioselective Biocatalyst;Advanced Synthesis & Catalysis;2019-03-06
3. Rh-Catalyzed Asymmetric Hydrogenation of β-Branched Enol Esters for the Synthesis of β-Chiral Primary Alcohols;Organic Letters;2017-12-08
4. Impact of variation of the acyl group on the efficiency and selectivity of the lipase-mediated resolution of 2-phenylalkanols;Tetrahedron: Asymmetry;2017-09
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