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Authordc.contributor.authorTapia, Ricardo A. 
Authordc.contributor.authorCarrasco, Claudia 
Authordc.contributor.authorOjeda, Scarlet 
Authordc.contributor.authorSalas, Cristian 
Authordc.contributor.authorValderrama, Jaime A. 
Authordc.contributor.authorMorello Casté, Antonio 
Authordc.contributor.authorRepetto Scaramelli, Yolanda 
Admission datedc.date.accessioned2018-12-20T15:20:33Z
Available datedc.date.available2018-12-20T15:20:33Z
Publication datedc.date.issued2002
Cita de ítemdc.identifier.citationJournal of Heterocyclic Chemistry, Volumen 39, Issue 5, 2018, Pages 1093-1096
Identifierdc.identifier.issn0022152X
Identifierdc.identifier.other10.1002/jhet.5570390540
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/158819
Abstractdc.description.abstractThe synthesis of new indazol-4,7-dione derivatives via 1,3-dipolar cycloaddition of diazomethane with 2,3-dimethyl-1,4-benzoquinone (2) and 1,4-naphthoquinone (7) followed by N-alkylation of the pyrazol nitrogen atom of the corresponding quinones (3) and (8) with methyl chloroacetate is described. A series of amides from esters (5) and (10) were also obtained. These compounds were tested in vitro as potential antitrypanosomal agents. Compounds (4) and (8) were found to have significant activity.
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.sourceJournal of Heterocyclic Chemistry
Keywordsdc.subjectOrganic Chemistry
Títulodc.titleSynthesis of indazol-4,7-dione derivatives as potential trypanocidal agents
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