A direct synthetic route to fused tricyclic quinolones from 2,3-diaminoquinolin-4(1 <i>H</i> )one

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dc.contributor.authorEnrique de J. Mauriño-Reyes
dc.contributor.authorEdgar González-Rodríguez
dc.contributor.authorFrancisco J. Reyes-Rangel
dc.contributor.authorAlfonso Lira‐Rocha
dc.contributor.authorMarco A. Loza-Mejía
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T15:58:34Z
dc.date.available2026-03-22T15:58:34Z
dc.date.issued2016
dc.descriptionCitaciones: 2
dc.description.abstractAbstract Fused tricyclic heterocycles are useful compounds in many areas of chemistry. In this study, 2,3-diaminoquinolin-4(1 H )one ( 5 ), a key intermediate for the preparation of tricyclic compounds, was prepared from isatoic anhydride in four steps with high yields under mild conditions and an easy workup, with most of the reactions carried out in aqueous medium. Compound 5 was transformed into a series of tricyclic fused products 8 and 9 .
dc.identifier.doi10.1515/hc-2016-0059
dc.identifier.urihttps://doi.org/10.1515/hc-2016-0059
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/55515
dc.language.isoen
dc.publisherDe Gruyter
dc.relation.ispartofHeterocyclic Communications
dc.sourceUniversidad La Salle
dc.subjectTricyclic
dc.subjectChemistry
dc.subjectCombinatorial chemistry
dc.subjectAqueous medium
dc.subjectOrganic chemistry
dc.subjectAqueous solution
dc.subjectStereochemistry
dc.titleA direct synthetic route to fused tricyclic quinolones from 2,3-diaminoquinolin-4(1 <i>H</i> )one
dc.typearticle

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