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Application of Enzyme- and Microorganism-catalyzed Reactions to Organic Synthesis

Application of Enzyme- and Microorganism-catalyzed Reactions to Organic Synthesis <jats:sec> <jats:title>Abstract:</jats:title> <jats:p>Three topics of recent achievements in the application of enzyme- and microorganism-catalyzed reactions to organic synthesis are focused. 1) Asymmetric synthesis and enantiomeric resolution, such as yeast-catalyzed asymmetric reduction of a carbonyl group and hydrolytic enzyme - catalyzed enantioselective hydrolysis of esters and transesterifica­ tion are described. Special emphasis is laid on the enzyme-catalyzed preparation of ex-hydroxy acids in enantiomerically enriched forms. Examples of enzyme-catalyzed asymmetric C-C bond formation are shortly commented. 2) The advantage of enzymatic hydrolysis of nitriles, amides, and esters are introduced, as the examples of the transformation of functional groups under mild condition. 3) The complementary use of chemical and enzymatic reaction in the total scheme is shown, in our synthesis of pyrenophorin and N-glycolylneuraminic acid.</jats:p> </jats:sec> http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Current Organic Chemistry CrossRef

Application of Enzyme- and Microorganism-catalyzed Reactions to Organic Synthesis

Current Organic Chemistry , Volume 3 (4): 373-406 – Jul 1, 1997

Application of Enzyme- and Microorganism-catalyzed Reactions to Organic Synthesis


Abstract

<jats:sec>
<jats:title>Abstract:</jats:title>
<jats:p>Three topics of recent achievements in the application of enzyme- and microorganism-catalyzed reactions to organic synthesis are focused. 1) Asymmetric synthesis and enantiomeric resolution, such as yeast-catalyzed asymmetric reduction of a carbonyl group and hydrolytic enzyme - catalyzed enantioselective hydrolysis of esters and transesterifica­
tion are described. Special emphasis is laid on the enzyme-catalyzed preparation of ex-hydroxy acids in enantiomerically enriched forms. Examples of enzyme-catalyzed asymmetric C-C bond formation are shortly commented. 2) The advantage of enzymatic hydrolysis of nitriles, amides, and esters are introduced, as the examples of the transformation of functional groups under mild condition. 3) The complementary use of chemical and enzymatic reaction in the total scheme is shown, in our synthesis of pyrenophorin and N-glycolylneuraminic acid.</jats:p>
</jats:sec>

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Publisher
CrossRef
ISSN
1385-2728
DOI
10.2174/1385272803666220202204517
Publisher site
See Article on Publisher Site

Abstract

<jats:sec> <jats:title>Abstract:</jats:title> <jats:p>Three topics of recent achievements in the application of enzyme- and microorganism-catalyzed reactions to organic synthesis are focused. 1) Asymmetric synthesis and enantiomeric resolution, such as yeast-catalyzed asymmetric reduction of a carbonyl group and hydrolytic enzyme - catalyzed enantioselective hydrolysis of esters and transesterifica­ tion are described. Special emphasis is laid on the enzyme-catalyzed preparation of ex-hydroxy acids in enantiomerically enriched forms. Examples of enzyme-catalyzed asymmetric C-C bond formation are shortly commented. 2) The advantage of enzymatic hydrolysis of nitriles, amides, and esters are introduced, as the examples of the transformation of functional groups under mild condition. 3) The complementary use of chemical and enzymatic reaction in the total scheme is shown, in our synthesis of pyrenophorin and N-glycolylneuraminic acid.</jats:p> </jats:sec>

Journal

Current Organic ChemistryCrossRef

Published: Jul 1, 1997

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