Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles

Detalhes bibliográficos
Autor(a) principal: Ferreira, Isabel C. F. R.
Data de Publicação: 2003
Outros Autores: Queiroz, Maria João R. P., Kirsch, Gilbert
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/58937
Resumo: New 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 systems
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spelling Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazolespalladiumaminationortho-bromodiarylaminescyclizationthienocarbazolesindolobenzo[b]thiophenesCiências Naturais::Ciências QuímicasScience & TechnologyNew 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 systemsThanks 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.info:eu-repo/semantics/publishedVersionElsevier LtdUniversidade do MinhoFerreira, Isabel C. F. R.Queiroz, Maria João R. P.Kirsch, Gilbert20032003-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/58937eng0040-402010.1016/S0040-4020(03)00552-0info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:46:45Zoai:repositorium.sdum.uminho.pt:1822/58937Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:44:46.886154Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
title Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
spellingShingle Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
Ferreira, Isabel C. F. R.
palladium
amination
ortho-bromodiarylamines
cyclization
thienocarbazoles
indolobenzo[b]thiophenes
Ciências Naturais::Ciências Químicas
Science & Technology
title_short Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
title_full Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
title_fullStr Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
title_full_unstemmed Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
title_sort Palladium-catalyzed amination and cyclization to heteroannellated indoles and carbazoles
author Ferreira, Isabel C. F. R.
author_facet Ferreira, Isabel C. F. R.
Queiroz, Maria João R. P.
Kirsch, Gilbert
author_role author
author2 Queiroz, Maria João R. P.
Kirsch, Gilbert
author2_role author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Ferreira, Isabel C. F. R.
Queiroz, Maria João R. P.
Kirsch, Gilbert
dc.subject.por.fl_str_mv palladium
amination
ortho-bromodiarylamines
cyclization
thienocarbazoles
indolobenzo[b]thiophenes
Ciências Naturais::Ciências Químicas
Science & Technology
topic palladium
amination
ortho-bromodiarylamines
cyclization
thienocarbazoles
indolobenzo[b]thiophenes
Ciências Naturais::Ciências Químicas
Science & Technology
description New 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 systems
publishDate 2003
dc.date.none.fl_str_mv 2003
2003-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/58937
url http://hdl.handle.net/1822/58937
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0040-4020
10.1016/S0040-4020(03)00552-0
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier Ltd
publisher.none.fl_str_mv Elsevier Ltd
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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