Synthesis of new 3-arylindole-2-carboxylates using beta,beta-diaryldehydroamino acids as building blocks. Fluorescence studies

Detalhes bibliográficos
Autor(a) principal: Queiroz, Maria João R. P.
Data de Publicação: 2007
Outros Autores: Abreu, Ana S., Castanheira, Elisabete M. S., Ferreira, Paula M. T.
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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spelling 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
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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