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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/39045

Title: Stereochemical Recognition in Lipase Catalysis
Authors: Ching-Shih Chen;Yeuk-Chuen Liu
Contributors: 國立臺灣海洋大學:食品科學系
Date: 1992
Issue Date: 2016-11-22T08:49:45Z
Publisher: Journal of Japan Oil Chemists' Society
Abstract: Abstract: Enantioselective lipase catalysis, in either aqueous or organic media, is becoming increasingly important in preparative synthetic chemistry. Despite poor enantiotopic selectivity in hydrolyzing triacylglycerols, lipases proved to be remarkable asymmetric agents in resolving carboxylic acids and alcohols. Thus, this article discusses (1) the general catalytic features of lipases, (2) the basic principles that govern the stereochemical selectivity of lipase catalysis in aqueous and organic media for the preparation of optically active compounds, and (3) experimental parameters important to lipase-catalyzed enantioselective esterification in organic solvents.
Relation: 41
URI: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/39045
Appears in Collections:[食品科學系] 期刊論文

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