Convenient Synthesis of 3-Vinyl and
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10174/3465 https://doi.org/10.1021/ol201983u |
Resumo: | A variety of 2-hydroxy aldehydes on reaction with 3-butenoic acid afford in a one-pot reaction the corresponding 3-vinylcoumarins. As expected, extension of the delocalized π-electron system accomplished by Heck coupling reactions with aryl halides results in an increased fluorescence of the compounds whose applicability is yet to be established. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Convenient Synthesis of 3-Vinyl and3-Vinyl Coumarins3-Styryl CoumarinsA variety of 2-hydroxy aldehydes on reaction with 3-butenoic acid afford in a one-pot reaction the corresponding 3-vinylcoumarins. As expected, extension of the delocalized π-electron system accomplished by Heck coupling reactions with aryl halides results in an increased fluorescence of the compounds whose applicability is yet to be established.Organic Letters/American Chemical Society2012-01-12T15:27:42Z2012-01-122011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/3465http://hdl.handle.net/10174/3465https://doi.org/10.1021/ol201983uengCQEndndndndamlp@uevora.ptndGordo, JoanaAvó, JoãoParola, JorgeLima, JoãoPereira, AntónioBranco, Paulainfo: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:10174/3465Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:58:57.001335Repositório 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 |
Convenient Synthesis of 3-Vinyl and |
title |
Convenient Synthesis of 3-Vinyl and |
spellingShingle |
Convenient Synthesis of 3-Vinyl and Gordo, Joana 3-Vinyl Coumarins 3-Styryl Coumarins |
title_short |
Convenient Synthesis of 3-Vinyl and |
title_full |
Convenient Synthesis of 3-Vinyl and |
title_fullStr |
Convenient Synthesis of 3-Vinyl and |
title_full_unstemmed |
Convenient Synthesis of 3-Vinyl and |
title_sort |
Convenient Synthesis of 3-Vinyl and |
author |
Gordo, Joana |
author_facet |
Gordo, Joana Avó, João Parola, Jorge Lima, João Pereira, António Branco, Paula |
author_role |
author |
author2 |
Avó, João Parola, Jorge Lima, João Pereira, António Branco, Paula |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Gordo, Joana Avó, João Parola, Jorge Lima, João Pereira, António Branco, Paula |
dc.subject.por.fl_str_mv |
3-Vinyl Coumarins 3-Styryl Coumarins |
topic |
3-Vinyl Coumarins 3-Styryl Coumarins |
description |
A variety of 2-hydroxy aldehydes on reaction with 3-butenoic acid afford in a one-pot reaction the corresponding 3-vinylcoumarins. As expected, extension of the delocalized π-electron system accomplished by Heck coupling reactions with aryl halides results in an increased fluorescence of the compounds whose applicability is yet to be established. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01-01T00:00:00Z 2012-01-12T15:27:42Z 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/10174/3465 http://hdl.handle.net/10174/3465 https://doi.org/10.1021/ol201983u |
url |
http://hdl.handle.net/10174/3465 https://doi.org/10.1021/ol201983u |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
CQE nd nd nd nd amlp@uevora.pt nd |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Organic Letters/American Chemical Society |
publisher.none.fl_str_mv |
Organic Letters/American Chemical Society |
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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1799136472282955776 |