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Synthesis of potential anti-tumoral ring a substituted tieno[3,2-c]carbazoles from diarylamines

dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorKirsch, Gilbert
dc.date.accessioned2011-03-22T15:18:44Z
dc.date.available2011-03-22T15:18:44Z
dc.date.issued2002
dc.description.abstractThienocarbazoles bearing electron donating or withdrawing groups in ring a, were prepared by intramolecular oxidative cyclization of diarylamines using stoichiometric or catalytic Pd(OAc)2 amounts, in fair to moderate yields. ln the latter case Cu(OAch was added to reoxidize Pd(O) forrned. The diarylamine precursors were prepared by palladium-catalysed amination.por
dc.identifier.citationFerreira, Isabel C.F.R.; Queiroz, Maria-João R.P.; Kirsch, Gilbert (2002). Synthesis of potential anti-tumoral ring a substituted tieno[3,2-c]carbazoles from diarylamines. In XXth European Colloqium on Heterocyclic Chemistry. Estocolmopor
dc.identifier.urihttp://hdl.handle.net/10198/3709
dc.language.isoengpor
dc.peerreviewedyespor
dc.titleSynthesis of potential anti-tumoral ring a substituted tieno[3,2-c]carbazoles from diarylaminespor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceEstocolmo, Suéciapor
oaire.citation.titleXXth European Colloqium on Heterocyclic Chemistrypor
person.familyNameFerreira
person.givenNameIsabel C.F.R.
person.identifier144781
person.identifier.ciencia-id9418-CF95-9919
person.identifier.orcid0000-0003-4910-4882
person.identifier.ridE-8500-2013
person.identifier.scopus-author-id36868826600
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
relation.isAuthorOfPublicationbd0d1537-2e03-41fb-b27a-140af9c35db8
relation.isAuthorOfPublication.latestForDiscoverybd0d1537-2e03-41fb-b27a-140af9c35db8

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