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dc.contributor.CRUESPUniversidade Estadual de Campinaspt_BR
dc.typeArtigo de periódicopt_BR
dc.titleC-H Functionalization of 1,4-Naphthoquinone by Oxidative Coupling with Anilines in the Presence of a Catalytic Quantity of Copper(II) Acetatept_BR
dc.contributor.authorLisboa, CDpt_BR
dc.contributor.authorSantos, VGpt_BR
dc.contributor.authorVaz, BGpt_BR
dc.contributor.authorde Lucas, NCpt_BR
dc.contributor.authorEberlin, MNpt_BR
dc.contributor.authorGarden, SJpt_BR
unicamp.author.emailgarden@iq.ufrj.brpt_BR
unicamp.authorLisboa, Cinthia da S. de Lucas, Nanci C. Garden, Simon J. Univ Fed Rio de Janeiro, Inst Quim, BR-21941909 Rio De Janeiro, RJ, Brazilpt_BR
unicamp.authorSantos, Vanessa G. Vaz, Boniek G. Eberlin, Marcos N. Univ Estadual Campinas UNICAMP, Inst Quim, Lab ThoMSon Espectrometria Massas, BR-13084971 Campinas, SP, Brazilpt_BR
dc.subject.wos(-)-cribrostatin-4 Renieramycin-hpt_BR
dc.subject.wosNaphthoquinone Coloring Matterspt_BR
dc.subject.wosElectronic Absorption-spectrapt_BR
dc.subject.wosIonization Mass-spectrometrypt_BR
dc.subject.wosMarine Spongept_BR
dc.subject.wosLavendamycin Analogspt_BR
dc.subject.wosQuinone Chemistrypt_BR
dc.subject.wosMetal-ionspt_BR
dc.subject.wosTetrahydroisoquinoline Alkaloidspt_BR
dc.subject.wosNucleophilic-substitutionpt_BR
dc.description.abstractThe oxidative addition of anilines (2) with 1,4-naphthoquinone (3) to give N-aryl-2-amino-1,4-naphthoquinones (1) was found to be catalyzed by copper(II) acetate. In the absence of the catalyst, the reactions are slower and give lower yields with the formation of many colateral products. In the presence of 10 mol % hydrated copper(II) acetate, the reactions are generally more efficient in that they are cleaner, higher yielding, and faster.pt
dc.relation.ispartofJournal Of Organic Chemistrypt_BR
dc.relation.ispartofabbreviationJ. Org. Chem.pt_BR
dc.publisher.cityWashingtonpt_BR
dc.publisher.countryEUApt_BR
dc.publisherAmer Chemical Socpt_BR
dc.date.issued2011pt_BR
dc.date.monthofcirculation37073pt_BR
dc.identifier.citationJournal Of Organic Chemistry. Amer Chemical Soc, v. 76, n. 13, n. 5264, n. 5273, 2011.pt_BR
dc.language.isoenpt_BR
dc.description.volume76pt_BR
dc.description.issuenumber13pt_BR
dc.description.firstpage5264pt_BR
dc.description.lastpage5273pt_BR
dc.rightsfechadopt_BR
dc.sourceWeb of Sciencept_BR
dc.identifier.issn0022-3263pt_BR
dc.identifier.wosidWOS:000291920900012pt_BR
dc.identifier.doi10.1021/jo200354upt_BR
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)pt_BR
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)pt_BR
dc.description.sponsorship1Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorship1Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)pt_BR
dc.date.available2014-07-30T16:51:36Z
dc.date.available2015-11-26T18:06:07Z-
dc.date.accessioned2014-07-30T16:51:36Z
dc.date.accessioned2015-11-26T18:06:07Z-
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dc.identifier.urihttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/62658
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/62658-
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