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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/129442
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dc.contributor.authorBartolomeu, Aloisio de Andrade-
dc.contributor.authorMenezes, Manoel Lima de-
dc.contributor.authorSilva-Filho, Luiz Carlos da-
dc.date.accessioned2015-10-21T21:06:32Z-
dc.date.accessioned2016-10-25T21:09:11Z-
dc.date.available2015-10-21T21:06:32Z-
dc.date.available2016-10-25T21:09:11Z-
dc.date.issued2015-01-01-
dc.identifierhttp://www.tandfonline.com/doi/abs/10.1080/00397911.2014.999341-
dc.identifier.citationSynthetic Communications. Philadelphia: Taylor &francis Inc, v. 45, n. 9, p. 1114-1126, 2015.-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/11449/129442-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/129442-
dc.description.abstractA multicomponent reaction of -naphthol, dimethyl malonate, and aromatic aldehydes in the presence of NbCl5 as promoter is described. Under similar conditions, aromatic aldehydes with different substituents exhibited different behaviors than -naphthol and dimethyl malonate. In these MCRs, 4-aryl-3,4-dihydrobenzo[f]coumarins are obtained as the major products (41-93%) and 14-aryl-14H-dibenzo[a,j]xanthenes as the minor products (1-38%).en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent1114-1126-
dc.language.isoeng-
dc.publisherTaylor &francis Inc-
dc.sourceWeb of Science-
dc.subject4-Aryl-3en
dc.subject4 dihydrobenzo[f]coumarinsen
dc.subjectChemoselectiveen
dc.subjectLewis aciden
dc.subjectMulticomponent reactionsen
dc.subjectNiobium pentachlorideen
dc.titleChemoselective condensationof beta-naphthol, dimethyl malonate, andaromatic aldehydes promoted by niobium pentachlorideen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSao Paulo State Univ UNESP, Dept Chem, Lab Organ Synth &Proc LaOSP, Fac Sci, BR-17033360 Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ UNESP, Dept Chem, Lab Organ Synth &Proc LaOSP, Fac Sci, BR-17033360 Sao Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: Procs. 2012/23821-7-
dc.description.sponsorshipIdFAPESP: 2013/08697-0-
dc.identifier.doihttp://dx.doi.org/10.1080/00397911.2014.999341-
dc.identifier.wosWOS:000351232300009-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofSynthetic Communications-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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