Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/58937

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dc.contributor.authorFerreira, Isabel C. F. R.por
dc.contributor.authorQueiroz, Maria João R. P.por
dc.contributor.authorKirsch, Gilbertpor
dc.date.accessioned2019-02-05T12:03:52Z-
dc.date.available2019-02-05T12:03:52Z-
dc.date.issued2003-
dc.identifier.issn0040-4020por
dc.identifier.urihttps://hdl.handle.net/1822/58937-
dc.description.abstractNew ortho-bromodiarylamines in the benzo[b]thiophene series were prepared by palladium-catalyzed amination, either in the benzene or in the thiophene ring. These were submitted to palladium-catalyzed cyclization, under different required conditions, to give several differently substituted thieno[3,2-c] or [2,3-b]carbazoles and indolo[3,2-b]benzo[b]thiophenes. This constitutes a novel synthetic route to both tetracyclic systemspor
dc.description.sponsorshipThanks are due to Foundation for the Science and Technology-IBQF-Univ. Minho (Portugal), to the Research Incitment Programme of the Calouste Gulbenkian Foundation (Portugal) for financial support and to Escola Superior Agrária-Instituto Politécnico de Bragança for supporting in part Isabel C. F. R. Ferreira PhD.por
dc.language.isoengpor
dc.publisherElsevier Ltdpor
dc.rightsopenAccesspor
dc.subjectpalladiumpor
dc.subjectaminationpor
dc.subjectortho-bromodiarylaminespor
dc.subjectcyclizationpor
dc.subjectthienocarbazolespor
dc.subjectindolobenzo[b]thiophenespor
dc.titlePalladium-catalyzed amination and cyclization to heteroannellated indoles and carbazolespor
dc.typearticlepor
dc.peerreviewedyespor
oaire.citationStartPage3737por
oaire.citationEndPage3743por
oaire.citationIssue21por
oaire.citationVolume59por
dc.identifier.doi10.1016/S0040-4020(03)00552-0por
dc.subject.fosCiências Naturais::Ciências Químicaspor
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalTetrahedronpor
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