The formation of pyrazolo[1,5‐<i>a</i>]pyrimidines by the reaction of 3‐(4‐chlorophenyl)pyrazol‐5‐amine with chalcones

dc.contributor.authorJairo Quiroga
dc.contributor.authorBraulio Insuasty
dc.contributor.authorRicardo Rincon
dc.contributor.authorMarina Larrahondo
dc.contributor.authorNorbert Hanold
dc.contributor.authorHerbert Meier
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T14:43:23Z
dc.date.available2026-03-22T14:43:23Z
dc.date.issued1994
dc.descriptionCitaciones: 33
dc.description.abstractAbstract Cyclocondensation reactions of the pyrazol‐5‐amine 1 and the 1‐aryl‐3‐phenyl‐2‐propen‐1‐ones 2a‐d yield the 6,7‐dihydropyrazolo[1,5‐ a ]pyrimidines 7a‐d . Whereas 7a‐c can be isolated in pure state, 7d is subjected to a spontaneous oxidation.
dc.identifier.doi10.1002/jhet.5570310606
dc.identifier.urihttps://doi.org/10.1002/jhet.5570310606
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/48168
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofJournal of Heterocyclic Chemistry
dc.sourceUniversidad de Los Andes
dc.subjectChemistry
dc.subjectAmine gas treating
dc.subjectYield (engineering)
dc.subjectAryl
dc.subjectMedicinal chemistry
dc.subjectOrganic chemistry
dc.titleThe formation of pyrazolo[1,5‐<i>a</i>]pyrimidines by the reaction of 3‐(4‐chlorophenyl)pyrazol‐5‐amine with chalcones
dc.typearticle

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