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Authordc.contributor.authorInsuasty, B. 
Authordc.contributor.authorSaitz Barría, Claudio es_CL
Authordc.contributor.authorInsuasty, H. es_CL
Authordc.contributor.authorQuiroga, J. es_CL
Authordc.contributor.authorJullian Matthaei, Carolina es_CL
Admission datedc.date.accessioned2011-06-14T20:01:14Z
Available datedc.date.available2011-06-14T20:01:14Z
Publication datedc.date.issued2000-03
Cita de ítemdc.identifier.citationJOURNAL OF HETEROCYCLIC CHEMISTRY 37 (2): 401-403es_CL
Identifierdc.identifier.issn0022-152X
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121286
General notedc.descriptionArtículo de publicación ISIes_CL
Abstractdc.description.abstractSeveral new 6-amino- and 6,8-dinmino-4-aryl-2,3-dihydropyrimido[4,5-b][1,4]diazepines were obtained from the reaction of 4,5,6-triaminopyrimidine 1a and 2,4,5,6-tetraaminopyrimidine 1b with one equivalent of 3-dimethylaminopropiophenones 2 in absolute ethanol. Structure analysis of 6-amino- and 6,8-diamino-4-aryl-2,3-dihydropyrimido[4,5-b][1,4]diazepines 3a-i, determined by detailed nmr measurements, reveals a high regioselectivity of this reaction.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherHETERO CORPORATIONes_CL
Keywordsdc.subject4,5-DIAMINO-1,6-DIHYDROPYRIMIDIN-6-ONESes_CL
Títulodc.titleReaction of 4,5,6-triaminopyrimidine and 2,4,5,6-tetraaminopyrimidine with 3-dimethylaminopropiophenones. Synthesis of new 4-aryl-2,3-dihydropyrimido[4,5-b][1,4]diazepineses_CL
Document typedc.typeArtículo de revista


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