Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies
Autor(a) principal: | |
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Data de Publicação: | 2007 |
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/1822/8370 |
Resumo: | Several new methyl 3-arylindole-2-carboxylates were synthesized in high yields using a metal-assisted [Pd(OAc)2/Cu(OAc)2, DMF, 130 oC] intramolecular C-N cyclization of beta,beta-diaryldehydroamino acids, developed by us, thus extending the scope of this reaction. The latter were obtained by a bis-Suzuki coupling of a beta,beta-dibromodehydroalanine with arylboronic acids bearing either electron-donating groups (EDGs) or electron-withdrawing groups (EWGs). We were able to establish general conditions for this coupling reaction [PdCl2dppf.CH2Cl2 1:1(20 mol%), boronic acid (5 equiv.), Cs2CO3 (1.4 equiv.), THF/H2O 1:1, 80 oC]. This strategy constitutes a novel, general and unprecedent approach to the synthesis of 3-arylindole-2-carboxylates. The fluorescence of the differently substituted indoles prepared was studied in several polar and non-polar solvents. In general the new indoles exhibit a solvent sensitive emission. The indoles with EDGs (OCH3 and SCH3) have reasonable fluorescence quantum yields in all solvents except in water. The indole with the cyano groups shows high fluorescent quantum yields in all solvents studied, despite the lower solvent sensitivity of its emission. The indole with the acetyl groups only exhibits reasonable fluorescence quantum yields in protic solvents. The fluorescence studies show that the new 3-arylindole-2-carboxylates are good candidates to be used as fluorescent probes. |
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Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studiesBeta,beta-diaryldehydroamino acidsBis-Suzuki couplingMetal-assisted C-N cyclization3-arylindole-2-carboxylatesFluorescenceFluorescent probesβ,β-Diaryldehydroamino acidsScience & TechnologySeveral new methyl 3-arylindole-2-carboxylates were synthesized in high yields using a metal-assisted [Pd(OAc)2/Cu(OAc)2, DMF, 130 oC] intramolecular C-N cyclization of beta,beta-diaryldehydroamino acids, developed by us, thus extending the scope of this reaction. The latter were obtained by a bis-Suzuki coupling of a beta,beta-dibromodehydroalanine with arylboronic acids bearing either electron-donating groups (EDGs) or electron-withdrawing groups (EWGs). We were able to establish general conditions for this coupling reaction [PdCl2dppf.CH2Cl2 1:1(20 mol%), boronic acid (5 equiv.), Cs2CO3 (1.4 equiv.), THF/H2O 1:1, 80 oC]. This strategy constitutes a novel, general and unprecedent approach to the synthesis of 3-arylindole-2-carboxylates. The fluorescence of the differently substituted indoles prepared was studied in several polar and non-polar solvents. In general the new indoles exhibit a solvent sensitive emission. The indoles with EDGs (OCH3 and SCH3) have reasonable fluorescence quantum yields in all solvents except in water. The indole with the cyano groups shows high fluorescent quantum yields in all solvents studied, despite the lower solvent sensitivity of its emission. The indole with the acetyl groups only exhibits reasonable fluorescence quantum yields in protic solvents. The fluorescence studies show that the new 3-arylindole-2-carboxylates are good candidates to be used as fluorescent probes.Fundação para a Ciência e a Tecnologia (FCT)ElsevierUniversidade do MinhoQueiroz, Maria João R. P.Abreu, Ana S.Castanheira, Elisabete M. S.Ferreira, Paula M. T.2007-012007-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/8370eng"Tetrahedron". ISSN 0040-4020. 63 (Jan. 2007) 2215-2222.0040-402010.1016/j.tet.2006.12.084www.sciencedirect.cominfo: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:RCAAP2023-07-21T12:32:59Zoai:repositorium.sdum.uminho.pt:1822/8370Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:28:26.049103Repositório 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 |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
title |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
spellingShingle |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies Queiroz, Maria João R. P. Beta,beta-diaryldehydroamino acids Bis-Suzuki coupling Metal-assisted C-N cyclization 3-arylindole-2-carboxylates Fluorescence Fluorescent probes β,β-Diaryldehydroamino acids Science & Technology |
title_short |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
title_full |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
title_fullStr |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
title_full_unstemmed |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
title_sort |
Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies |
author |
Queiroz, Maria João R. P. |
author_facet |
Queiroz, Maria João R. P. Abreu, Ana S. Castanheira, Elisabete M. S. Ferreira, Paula M. T. |
author_role |
author |
author2 |
Abreu, Ana S. Castanheira, Elisabete M. S. Ferreira, Paula M. T. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Queiroz, Maria João R. P. Abreu, Ana S. Castanheira, Elisabete M. S. Ferreira, Paula M. T. |
dc.subject.por.fl_str_mv |
Beta,beta-diaryldehydroamino acids Bis-Suzuki coupling Metal-assisted C-N cyclization 3-arylindole-2-carboxylates Fluorescence Fluorescent probes β,β-Diaryldehydroamino acids Science & Technology |
topic |
Beta,beta-diaryldehydroamino acids Bis-Suzuki coupling Metal-assisted C-N cyclization 3-arylindole-2-carboxylates Fluorescence Fluorescent probes β,β-Diaryldehydroamino acids Science & Technology |
description |
Several new methyl 3-arylindole-2-carboxylates were synthesized in high yields using a metal-assisted [Pd(OAc)2/Cu(OAc)2, DMF, 130 oC] intramolecular C-N cyclization of beta,beta-diaryldehydroamino acids, developed by us, thus extending the scope of this reaction. The latter were obtained by a bis-Suzuki coupling of a beta,beta-dibromodehydroalanine with arylboronic acids bearing either electron-donating groups (EDGs) or electron-withdrawing groups (EWGs). We were able to establish general conditions for this coupling reaction [PdCl2dppf.CH2Cl2 1:1(20 mol%), boronic acid (5 equiv.), Cs2CO3 (1.4 equiv.), THF/H2O 1:1, 80 oC]. This strategy constitutes a novel, general and unprecedent approach to the synthesis of 3-arylindole-2-carboxylates. The fluorescence of the differently substituted indoles prepared was studied in several polar and non-polar solvents. In general the new indoles exhibit a solvent sensitive emission. The indoles with EDGs (OCH3 and SCH3) have reasonable fluorescence quantum yields in all solvents except in water. The indole with the cyano groups shows high fluorescent quantum yields in all solvents studied, despite the lower solvent sensitivity of its emission. The indole with the acetyl groups only exhibits reasonable fluorescence quantum yields in protic solvents. The fluorescence studies show that the new 3-arylindole-2-carboxylates are good candidates to be used as fluorescent probes. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-01 2007-01-01T00:00:00Z |
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/1822/8370 |
url |
http://hdl.handle.net/1822/8370 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
"Tetrahedron". ISSN 0040-4020. 63 (Jan. 2007) 2215-2222. 0040-4020 10.1016/j.tet.2006.12.084 www.sciencedirect.com |
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 |
publisher.none.fl_str_mv |
Elsevier |
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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799132779901878272 |