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Palladium-catalyzed amination to obtain o-halodiarylamines precursors of thienocarbazoles

dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorKirsch, Gilbert
dc.date.accessioned2011-02-10T11:42:23Z
dc.date.available2011-02-10T11:42:23Z
dc.date.issued2001
dc.description.abstractWith the aim of obtaining potential anti-tumoural thienocarbazoles by a ring B convergent method of synthesis, o-halodiarylacetamides were prepared by copper assisted C-N coupling from 2-bromo-iodobenzene and 6-acetamido-2,3,5-trimethylbenzo[b]thiophene, prepared from the 6-acetyl compound.
dc.description.abstracto-Bromodiarylamines l were prepared by palladium-catalyzed amination of 2-bromo-iodobenzene or 6-bromobenzo[b]thiophenes, using Buchwald conditions.
dc.identifier.citationFerreira, Isabel C.F.R.; Queiroz, Maria-João R.P.; Kirsch, Gilbert (2001). Palladium-catalyzed amination to obtain o-halodiarylamines precursors of thienocarbazoles. In 12th European Symposium on Organic Chemistry. Groningenpor
dc.identifier.urihttp://hdl.handle.net/10198/3323
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherESOCpor
dc.titlePalladium-catalyzed amination to obtain o-halodiarylamines precursors of thienocarbazolespor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceGroningen, Holandapor
oaire.citation.title12th European Symposium on Organic 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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