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Epoxide hydrolase-catalyzed enantioselective synthesis of chiral 1,2-diols via desymmetrization of meso-epoxides. lzhao@diversa.com.
Zhao, Lishan; Han, Bin; Huang, Zilin; Miller, Mark; Huang, Hongjun; Malashock, Dan S; Zhu, Zuolin; Milan, Aileen; Robertson, Dan E; Weiner, David P; Burk, Mark J.
Afiliação
  • Zhao L; Diversa Corporation, 4955 Directors Place, San Diego, California 92121, USA. lzhao@diversa.com
J Am Chem Soc ; 126(36): 11156-7, 2004 Sep 15.
Article em En | MEDLINE | ID: mdl-15355089
The discovery, from nature, of a diverse set of microbial epoxide hydrolases is reported. The utility of a library of epoxide hydrolases in the synthesis of chiral 1,2-diols via desymmetrization of a wide range of meso-epoxides, including cyclic as well as acyclic alkyl- and aryl-substituted substrates, is demonstrated. The chiral (R,R)-diols were furnished with high ee's and yields. The discovery of the first microbial epoxide hydrolases providing access to complementary (S,S)-diols is also described.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Álcoois / Epóxido Hidrolases / Compostos de Epóxi Idioma: En Revista: J Am Chem Soc Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Álcoois / Epóxido Hidrolases / Compostos de Epóxi Idioma: En Revista: J Am Chem Soc Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Estados Unidos