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Enantioselective protonation.
Mohr, Justin T; Hong, Allen Y; Stoltz, Brian M.
Afiliación
  • Mohr JT; Arnold and Mabel Beckman Laboratories of Chemical Synthesis, Department of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Mail Code 164-30, Pasadena, CA 91125, USA.
Nat Chem ; 1(5): 359-69, 2009 Aug.
Article en En | MEDLINE | ID: mdl-20428461
ABSTRACT
Enantioselective protonation is a common process in biosynthetic sequences. The decarboxylase and esterase enzymes that effect this valuable transformation are able to control both the steric environment around the proton acceptor (typically an enolate) and the proton donor (typically a thiol). Recently, several chemical methods to achieve enantioselective protonation have been developed by exploiting various means of enantiocontrol in different mechanisms. These laboratory transformations have proven useful for the preparation of a number of valuable organic compounds.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Protones Idioma: En Revista: Nat Chem Asunto de la revista: QUIMICA Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Protones Idioma: En Revista: Nat Chem Asunto de la revista: QUIMICA Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos