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Authordc.contributor.authorEscobar, Carlos A. 
Authordc.contributor.authorDonoso Tauda, Oscar 
Authordc.contributor.authorAraya Maturana, Ramiro 
Authordc.contributor.authorSicker, Dieter 
Admission datedc.date.accessioned2018-12-20T14:12:14Z
Available datedc.date.available2018-12-20T14:12:14Z
Publication datedc.date.issued2009
Cita de ítemdc.identifier.citationSynthetic Communications, Volumen 39, Issue 1, 2018, Pages 166-174
Identifierdc.identifier.issn00397911
Identifierdc.identifier.issn15322432
Identifierdc.identifier.other10.1080/00397910802372517
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/154687
Abstractdc.description.abstract1,5-Benzodiazepines have been synthesized from the corresponding 2'-hydroxychalcones [1-(2-hydroxyphenyl)-3-aryl-2-propen-1-ones] and o-phenylenediamine, both in methanol, under reflux and under solvent-free microwave irradiation conditions on alumina. The latter method proved to be advantageous. Copyright © Taylor & Francis Group, LLC.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceSynthetic Communications
Keywordsdc.subjectAlumina
Keywordsdc.subjectBenzodiazepine
Keywordsdc.subjectChalcone
Keywordsdc.subjectMicrowave irradiation
Keywordsdc.subjectSolvent-free synthesis
Títulodc.titleSynthesis of 1,5-benzodiazepines with unusual substitution pattern from chalcones under solvent-free microwave irradiation conditions
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile