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Authordc.contributor.authorLezana Tobar, Nicolás 
Authordc.contributor.authorMatus Pérez, Massiel 
Authordc.contributor.authorGaldámez Silva, Antonio 
Authordc.contributor.authorLuehr, Susan 
Authordc.contributor.authorVilches Herrer, Marcelo 
Admission datedc.date.accessioned2016-12-06T13:51:26Z
Available datedc.date.available2016-12-06T13:51:26Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationGreen Chemistry Volumen: 18 Número: 13 Páginas: 3712-3717es_ES
Identifierdc.identifier.other10.1039/c6gc00912c
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/141678
Abstractdc.description.abstractA microwave-assisted method for the synthesis of tetracyclic tetra-hydropyridines via an intramolecular imino-Diels-Alder reaction in water is reported. The reaction proceeds under catalyst-free conditions and shows excellent stereoselectivityes_ES
Patrocinadordc.description.sponsorshipCONICYT 821320027es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherRoyal Society of Chemistryes_ES
Sourcedc.sourceGreen Chemistryes_ES
Keywordsdc.subjectN-arylimineses_ES
Keywordsdc.subjectOne-potes_ES
Keywordsdc.subjectDerivativeses_ES
Keywordsdc.subject1-aza-1,3-butadienees_ES
Keywordsdc.subjectHeterocycleses_ES
Keywordsdc.subjectMechanismes_ES
Keywordsdc.subjectAldehydeses_ES
Títulodc.titleHighly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels-Alder reaction under microwave irradiation in wateres_ES
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatoses_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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