Synthesis of substituted flavones and arylchromones using P and Si Keggin heteropolyacids as catalysts

A simple and clean procedure for the preparation of functionalized flavones and chromones using commercial Keggin heteropolyacid in acetonitrile medium is described for the cyclization of l-(2- hydroxyaiyl)-3-aryl-l,3-propanodiones. Sixteen examples are reported, yields ranging in 60-91%; five subst...

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Autores principales: Bennardi, Daniel Oscar, Romanelli, Gustavo Pablo, Jios, Jorge Luis, Vázquez, Patricia Graciela, Cáceres, Carmen V., Autino, Juan Carlos
Formato: Articulo Comunicacion
Lenguaje:Inglés
Publicado: 2007
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Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/120067
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Sumario:A simple and clean procedure for the preparation of functionalized flavones and chromones using commercial Keggin heteropolyacid in acetonitrile medium is described for the cyclization of l-(2- hydroxyaiyl)-3-aryl-l,3-propanodiones. Sixteen examples are reported, yields ranging in 60-91%; five substituted 2-naphthyIchromones are prepared for the first time.