An efficient synthesis of optically active metabolites of platelet adhesion inhibitor OPC-29030 by lipase-catalyzed enantioselective transesterification-Reference-Cited by-同舟云学术

An efficient synthesis of optically active metabolites of platelet adhesion inhibitor OPC-29030 by lipase-catalyzed enantioselective transesterification

Published:1999-07 Issue:28 Volume:40 Page:5235-5238
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kitano Kazuyoshi,Matsubara Jun,Ohtani Tadaaki,Otsubo Kenji,Kawano Yoshikazu,Morita Seiji,Uchida Minoru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Synthesis of 2(1H)-Quinolinone Derivatives and Their Inhibitory Activity on the Release of 12(S)-Hydroxyeicosatetraenoic Acid (12-HETE) from Platelets.

2. Facile enzymatic preparation of enantiomeric .BETA.-lactams.

3. Lipase-Catalyzed Enantioselective Synthesis of Optically Active Mephobarbital, Hexobarbital and Febarbamate.

4. Enzymatic synthesis of optically active 2-carbamoyl-oxymethyl-1,4-dihydropyridines, (R)-(+)- and (S)-(−)-NB 818

5. Oxalate as an activated ester group in lipase-catalyzed enantioselective hydrolysis: A versatile approach to d-α-tocopherol

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