New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions

Detalhes bibliográficos
Autor(a) principal: Martins, Sérgio
Data de Publicação: 2010
Outros Autores: Branco, Paula, Torre, Maria, Sierra, Miguel, Pereira, António
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/3464
https://doi.org/10.1055/s-0030-1259014
Resumo: A particularly useful, easy and concise synthesis of diversified 3-aryl coumarin was achieved using Heck coupling reactions between coumarin and aryliodides. The introduction of the aryl moiety occurred regioselective at the 3-position of the heteroaromatic ring.
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spelling New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling ReactionscoumarinHeck reaction3-aryl coumarincoupling reactionA particularly useful, easy and concise synthesis of diversified 3-aryl coumarin was achieved using Heck coupling reactions between coumarin and aryliodides. The introduction of the aryl moiety occurred regioselective at the 3-position of the heteroaromatic ring.Synlett/Thieme2012-01-12T15:27:05Z2012-01-122010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/3464http://hdl.handle.net/10174/3464https://doi.org/10.1055/s-0030-1259014porCQEndndndndamlp@uevora.pt307Martins, SérgioBranco, PaulaTorre, MariaSierra, MiguelPereira, Antónioinfo: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:RCAAP2024-01-03T18:40:42Zoai:dspace.uevora.pt:10174/3464Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:58:56.908770Repositório 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 New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
title New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
spellingShingle New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
Martins, Sérgio
coumarin
Heck reaction
3-aryl coumarin
coupling reaction
title_short New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
title_full New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
title_fullStr New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
title_full_unstemmed New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
title_sort New Methodology for the Synthesis of 3-Substituted Coumarins via Pd-Catalyzed Site-Selective Cross-Coupling Reactions
author Martins, Sérgio
author_facet Martins, Sérgio
Branco, Paula
Torre, Maria
Sierra, Miguel
Pereira, António
author_role author
author2 Branco, Paula
Torre, Maria
Sierra, Miguel
Pereira, António
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Martins, Sérgio
Branco, Paula
Torre, Maria
Sierra, Miguel
Pereira, António
dc.subject.por.fl_str_mv coumarin
Heck reaction
3-aryl coumarin
coupling reaction
topic coumarin
Heck reaction
3-aryl coumarin
coupling reaction
description A particularly useful, easy and concise synthesis of diversified 3-aryl coumarin was achieved using Heck coupling reactions between coumarin and aryliodides. The introduction of the aryl moiety occurred regioselective at the 3-position of the heteroaromatic ring.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01T00:00:00Z
2012-01-12T15:27:05Z
2012-01-12
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/10174/3464
http://hdl.handle.net/10174/3464
https://doi.org/10.1055/s-0030-1259014
url http://hdl.handle.net/10174/3464
https://doi.org/10.1055/s-0030-1259014
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv CQE
nd
nd
nd
nd
amlp@uevora.pt
307
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Synlett/Thieme
publisher.none.fl_str_mv Synlett/Thieme
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
institution RCAAP
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
repository.mail.fl_str_mv
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