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Synthesis of diarylamines in the benzo[b]thiophene series by palladium-catalyzed amination and structure-activity relationship as antibacterial agents

dc.contributor.authorQueiroz, Maria João R.P.
dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorBarbosa, Sandra
dc.contributor.authorCalhelha, Ricardo C.
dc.contributor.authorEstevinho, Leticia M.
dc.date.accessioned2011-03-23T11:55:44Z
dc.date.available2011-03-23T11:55:44Z
dc.date.issued2004
dc.description.abstractThe palladium-catalyzed amination of arylhalides has become an important method for the synthesis of arylamines found in pharmaceuticals. Using this methodology we were able to synthesize several diarylamines in the benzo[b]thiophene series.Here we report the synthesis 01 differently substituted diarylamines derivatives 01 6-bromo or 6-amino- 2,3,5-trimethylbenzo[b]thiophene in good to high yields (50-90%) (Scheme), The amino precursor was prepared from the bromo compound using also a C-N palladium-catalyzed cross-coupling with benzophenone imine, followed by acidic hydrolysis in a 60% overall yield.por
dc.identifier.citationQueiroz, Maria-João R.P.; Ferreira, Isabel C.F.R.; Barbosa, Sandra; Calhelha, Ricardo; Estevinho, Letícia (2004). Synthesis of diarylamines in the benzo[b]thiophene series by palladium-catalyzed amination and structure-activity relationship as antibacterial agents. In International Symposium on Advances in Synthetic, Combinatorial and Medicinal Chemistry. Moscovopor
dc.identifier.urihttp://hdl.handle.net/10198/3728
dc.language.isoengpor
dc.peerreviewedyespor
dc.titleSynthesis of diarylamines in the benzo[b]thiophene series by palladium-catalyzed amination and structure-activity relationship as antibacterial agentspor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceMoscovo, Rússiapor
oaire.citation.titleInternational Symposium on Advances in Synthetic, Combinatorial and Medicinal Chemistrypor
person.familyNameFerreira
person.familyNameCalhelha
person.familyNameEstevinho
person.givenNameIsabel C.F.R.
person.givenNameRicardo C.
person.givenNameLetícia M.
person.identifier144781
person.identifier.ciencia-id9418-CF95-9919
person.identifier.ciencia-idF313-E3CE-554E
person.identifier.ciencia-idBA14-09D6-A406
person.identifier.orcid0000-0003-4910-4882
person.identifier.orcid0000-0002-6801-4578
person.identifier.orcid0000-0002-9249-1948
person.identifier.ridE-8500-2013
person.identifier.ridJ-2172-2014
person.identifier.scopus-author-id36868826600
person.identifier.scopus-author-id6507978333
person.identifier.scopus-author-id6506577664
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor
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relation.isAuthorOfPublication.latestForDiscovery2d5d1a41-7561-4a01-871c-b4c97da35053

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