dc.creatorAmarante, GW
dc.creatorBenassi, M
dc.creatorSabino, AA
dc.creatorEsteves, PM
dc.creatorCoelho, F
dc.creatorEberlin, MN
dc.date2006
dc.date44136
dc.date2014-11-19T21:52:42Z
dc.date2015-11-26T16:30:12Z
dc.date2014-11-19T21:52:42Z
dc.date2015-11-26T16:30:12Z
dc.date.accessioned2018-03-28T23:11:14Z
dc.date.available2018-03-28T23:11:14Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 47, n. 47, n. 8427, n. 8431, 2006.
dc.identifier0040-4039
dc.identifierWOS:000241910200051
dc.identifier10.1016/j.tetlet.2006.09.037
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/67062
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/67062
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/67062
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1269915
dc.descriptionA new mechanistic proposal on the formation of N-oxide hydroxyquinolines from BH adducts based on the interception by electrospray ionization mass spectrometry of a new key o-trifluoroacetylated intermediate. (c) 2006 Elsevier Ltd. All rights reserved.
dc.description47
dc.description47
dc.description8427
dc.description8431
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectElectrospray-ionization Mass
dc.subjectRadical-chain Reactions
dc.subjectHeck Reaction
dc.subjectStereoselective-synthesis
dc.subjectSpectrometry
dc.subjectDerivatives
dc.subjectAcid
dc.subjectQuinolines
dc.subjectMechanism
dc.subjectNitrobenzaldehydes
dc.titleFormation of substituted N-oxide hydroxyquinolines from o-nitrophenyl Baylis-Hillman adduct: a new key intermediate intercepted by ESI-(+)-MS(/MS) monitoring
dc.typeArtículos de revistas


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