Synthesis of enantiomerically pure (S)-mandelic acid using an oxynitrilase–nitrilase bienzymatic cascade: a nitrilase surprisingly shows nitrile hydratase activity-Reference-Cited by-同舟云学术

Synthesis of enantiomerically pure (S)-mandelic acid using an oxynitrilase–nitrilase bienzymatic cascade: a nitrilase surprisingly shows nitrile hydratase activity

Published:2006-02 Issue:3 Volume:17 Page:320-323
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Mateo Cesar,Chmura Andrzej,Rustler Sven,van Rantwijk Fred,Stolz Andreas,Sheldon Roger A.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference16 articles.

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2. Yamaguchi, Y.; Ushigome, M.; Kato, T. (Nitto Chem. Ind.), EP 773297, 1997 [Chem. Abstr. 1997, 127, 4190].

3. Endo, T.; Tamura, K. (Nitto Chem. Ind.), EP 449648, 1991 [Chem. Abstr. 1992, 116, 5338].

4. Oxynitrilases: From Cyanogenesis to Asymmetric Synthesis

5. Synthesis of (R)-cyanohydrins by crude (R)-oxynitrilase-catalyzed reactions in micro-aqueous medium

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