dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:55:18Z
dc.date.available2018-12-11T16:55:18Z
dc.date.created2018-12-11T16:55:18Z
dc.date.issued2018-10-18
dc.identifierTetrahedron, v. 74, n. 42, p. 6144-6149, 2018.
dc.identifier1464-5416
dc.identifier0040-4020
dc.identifierhttp://hdl.handle.net/11449/171432
dc.identifier10.1016/j.tet.2018.09.003
dc.identifier2-s2.0-85053054891
dc.description.abstractThis paper describes an original one-pot way to synthesize nine new halogenated aminoquinoline derivatives using reactions conducted by niobium pentachloride. Subsequently, we describe an efficient and selective reduction reaction of nitroquinolines using niobium pentachloride and zinc, producing important compounds in the organic synthesis. The results showed that it is an important tool to synthesize these compounds, besides being time- and resources-saving and generating good yields. A quick study of acidochromism was performed.
dc.languageeng
dc.relationTetrahedron
dc.relation0,800
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectAminoquinoline derivatives
dc.subjectNiobium pentachloride
dc.subjectOne-pot reactions
dc.subjectSelective reduction reactions
dc.titleNbCl5 a multifunctional reagent for the synthesis of new halogenated aminoquinoline compounds through innovative one-pot reaction and the acidochromism effect
dc.typeArtículos de revistas


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