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Silver-mediated fluorination of functionalized aryl stannanes.
Furuya, Takeru; Strom, Alexandra E; Ritter, Tobias.
Afiliación
  • Furuya T; Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts, USA.
J Am Chem Soc ; 131(5): 1662-3, 2009 Feb 11.
Article en En | MEDLINE | ID: mdl-19191693
ABSTRACT
We report a regiospecific silver-mediated fluorination of aryl stannanes. The presented reaction can afford complex fluoroarenes from readily available phenols in three steps. The operational simplicity and the broad substrate scope of the fluorination should render this reaction a useful tool for the synthesis of milligram to gram quantities of functionalized aryl fluorides. Silver-mediated oxidative transformations of aryl nucleophiles that proceed via bimetallic redox processes are a new avenue to develop carbon-heteroatom bond formations.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plata / Derivados del Benceno / Compuestos de Estaño / Hidrocarburos Fluorados Idioma: En Revista: J Am Chem Soc Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plata / Derivados del Benceno / Compuestos de Estaño / Hidrocarburos Fluorados Idioma: En Revista: J Am Chem Soc Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos