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Authordc.contributor.authorQuiroga, J. 
Authordc.contributor.authorInsuasty, B. es_CL
Authordc.contributor.authorHormaza, Angela es_CL
Authordc.contributor.authorSaitz Barría, Claudio es_CL
Authordc.contributor.authorJullian Matthaei, Carolina es_CL
Admission datedc.date.accessioned2011-06-21T14:18:52Z
Available datedc.date.available2011-06-21T14:18:52Z
Publication datedc.date.issued1998-05
Cita de ítemdc.identifier.citationJOURNAL OF HETEROCYCLIC CHEMISTRY 35 (3): 575-578es_CL
Identifierdc.identifier.issn0022-152X
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121316
General notedc.descriptionArtículo de publicación ISIes_CL
Abstractdc.description.abstractReaction of 5-amino-3-methyl-1-phenylpyrazole (1a) and 5-amino-3-(4-chlorophenyl)-1H-pyrazole (1b) with dimedone (2) and p-susbstituted benzaldehydes 3 in ethanol, afforded in all cases tricyclic linear 4-aryl- 7,7-dimethyl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b] quinolin-5-ones (4a-j) in good yields. The linear structures and hence the regiospecificity of the reaction were established by nmr measurements.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherHETERO CORPORATIONes_CL
Keywordsdc.subjectQuinoneses_CL
Títulodc.titleSynthesis of 4-aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-oneses_CL
Document typedc.typeArtículo de revista


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