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Authordc.contributor.authorIturriaga-Vásquez, Patricio 
Authordc.contributor.authorLühr Sierra, Susan es_CL
Authordc.contributor.authorCaroli Rezende, Marcos es_CL
Authordc.contributor.authorCassels Niven, Brucees_CL
Admission datedc.date.accessioned2009-04-09T12:40:10Z
Available datedc.date.available2009-04-09T12:40:10Z
Publication datedc.date.issued2006-03
Cita de ítemdc.identifier.citationJOURNAL OF THE CHILEAN CHEMICAL SOCIETY Volume: 51 Issue: 1 Pages: 781-783 Published: MAR 2006en
Identifierdc.identifier.issn0717-9324
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118809
Abstractdc.description.abstractA simple synthetic route for the preparation of 2-phenyl-1,3-propanediamines, based on a Knoevenagel-Michael double condensation followed by reduction, was developed using nitromethane as reagent and solvent, and sodium bicarbonate as base in the first step, followed by catalytic hydrogenation over Adams catalyst.en
Lenguagedc.language.isoenen
Publisherdc.publisherSOCIEDAD CHILENA DE QUIMICAen
Keywordsdc.subjectKnoevenagel-Michael double condensationen
Títulodc.titleSynthesis of 2-aryl-1,3-propanediamines using a one-pot Knoevenagel-Michael sequenceen
Document typedc.typeArtículo de revista


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