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Authordc.contributor.authorInsuasty O, Braulio 
Authordc.contributor.authorInsuasty I, Henry 
Authordc.contributor.authorQuiroga P, Jairo 
Authordc.contributor.authorSaitz Barría, Claudio 
Authordc.contributor.authorJullian Matthaei, Carolina 
Admission datedc.date.accessioned2018-12-20T15:04:10Z
Available datedc.date.available2018-12-20T15:04:10Z
Publication datedc.date.issued2000
Cita de ítemdc.identifier.citationJournal of Heterocyclic Chemistry, Volumen 37, Issue 2, 2018, Pages 401-403
Identifierdc.identifier.issn0022152X
Identifierdc.identifier.other10.1002/jhet.5570370228
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/157472
Abstractdc.description.abstractSeveral new 6-amino- and 6,8-diamino-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.
Lenguagedc.language.isoen
Publisherdc.publisherHeteroCorporation
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceJournal of Heterocyclic Chemistry
Keywordsdc.subjectOrganic Chemistry
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]diazepines
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