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Synthesis of thienocarbazoles by reductive cyclization of 6-(2’- nitrophenyl)benzo[b]thiophenes

dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorKirsch, Gilbert
dc.date.accessioned2011-02-10T12:17:27Z
dc.date.available2011-02-10T12:17:27Z
dc.date.issued2000
dc.description.abstractThienocarbazoles are bioisosters of anti-tumoural pyridocarbazoles, ellipticine and olivacine. Methylated thienocarbazoles 1 were synthesized by reductive cyclization of 6-(2'nitrophenyl) benzo[b]thiophenes 2, using triethylphosphite. Compounds 2 were obtained by palladium-catalyzed cross-coupling between 2-bromo or iodonitrobenzenes and 6-boronic esters of methylated benzo[b]thiophenes (communication presented at this meeting).
dc.identifier.citationFerreira, Isabel C.F.R.; Queiroz, Maria-João R.P.; Kirsch, Gilbert (2000) – Synthesis of thienocarbazoles by reductive cyclization of 6-(2’- nitrophenyl)benzo[b]thiophenes. In XIX th European Colloquium on Heterocyclic Chemistry. Aveiropor
dc.identifier.urihttp://hdl.handle.net/10198/3327
dc.language.isoengpor
dc.peerreviewedyespor
dc.titleSynthesis of thienocarbazoles by reductive cyclization of 6-(2’- nitrophenyl)benzo[b]thiophenespor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceAveiro, Portugalpor
oaire.citation.titleXIX th European Colloquium 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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