Synthesis of Biginelli adducts using a Preyssler heteropolyacid in silica matrix from biomass building block

An efficient, suitable and high yielding method has been developed employing the use of the renewable platform molecule furfural for the synthesis of Biginelli derivatives via a three-component domino reaction through a combination of aldehydes (furfural), β-ketoesters, and urea or thiourea using Pr...

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Detalles Bibliográficos
Autores: Portilla Zúñiga, Omar Miguel, Sathicq, Angel Gabriel, Martínez, José J., Fernandes, Sergio A., Rezende, Terezinha R. M., Romanelli, Gustavo Pablo
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2018
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/85215
Acceso en línea:http://hdl.handle.net/11336/85215
Access Level:acceso abierto
Palabra clave:BIGINELLI ADDUCTS
BIOMASS BUILDING BLOCK
FURFURAL DERIVATIVES
MICROWARE SYNTHESIS
MULTICOMPONENT REACTIONS
PREYSSLER CATALYST
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Descripción
Sumario:An efficient, suitable and high yielding method has been developed employing the use of the renewable platform molecule furfural for the synthesis of Biginelli derivatives via a three-component domino reaction through a combination of aldehydes (furfural), β-ketoesters, and urea or thiourea using Preyssler heteropolyacid H14NaP5W29MoO110 encapsulated in a silica framework as the catalyst. The reaction was carried out under solvent-free conditions, affording very good yields using thermal and microwave heating. Atom economy, an environmentally benign procedure, reuse of catalysts, and short reaction time are some of the important features of this protocol. The Preyssler catalyst embedded in the silica matrix is insoluble in polar and apolar media, which allows easy removal of the reaction products without affecting its catalytic activity.