Epoxide hydrolase-catalyzed enantioselective synthesis of chiral 1,2-diols via desymmetrization of meso-epoxides. 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.
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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