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Preparation of 5-substituted 1H-tetrazoles from nitriles in water.
Demko, Z P; Sharpless, K B.
Afiliación
  • Demko ZP; Department of Chemistry and The Skaggs Institute of Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Org Chem ; 66(24): 7945-50, 2001 Nov 30.
Article en En | MEDLINE | ID: mdl-11722189
ABSTRACT
The addition of sodium azide to nitriles to give 1H-tetrazoles is shown to proceed readily in water with zinc salts as catalysts. The scope of the reaction is quite broad; a variety of aromatic nitriles, activated and unactivated alkyl nitriles, substituted vinyl nitriles, thiocyanates, and cyanamides have all been shown to be viable substrates for this reaction.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetrazoles / Nitrilos Idioma: En Revista: J Org Chem Año: 2001 Tipo del documento: Article País de afiliación: Estados Unidos
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetrazoles / Nitrilos Idioma: En Revista: J Org Chem Año: 2001 Tipo del documento: Article País de afiliación: Estados Unidos