Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes

Detalhes bibliográficos
Autor(a) principal: Marinho, Elina Margarida Ribeiro
Data de Publicação: 2016
Outros Autores: Proença, M. Fernanda R. P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/51932
Resumo: 2-(2-Aminophenyl)quinazoline-4-amine, prepared from a quinazolino[3,4-a]quinazoline, were reacted with aromatic aldehydes under conventional heating or microwave irradiation, leading to high yields of tetracyclic dihydroquinazolines.
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spelling Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes2-(2-amino)quinazoline-4-aminearomatic aldehydesCiências Naturais::Ciências QuímicasScience & Technology2-(2-Aminophenyl)quinazoline-4-amine, prepared from a quinazolino[3,4-a]quinazoline, were reacted with aromatic aldehydes under conventional heating or microwave irradiation, leading to high yields of tetracyclic dihydroquinazolines.We gratefully acknowledge the financial support by the University of Minho and FCT through the Portuguese NMR network (RNRMN), the Project F-COMP-01-00124-FEDER-022716 (ref. FCT PEst-C/QUI/UI0686/2011) FEDER-COMPETE, and a PhD grant awarded to Elina Marinho (SFRH/BD/73659/2010).info:eu-repo/semantics/publishedVersionRoyal Society of ChemistryUniversidade do MinhoMarinho, Elina Margarida RibeiroProença, M. Fernanda R. P.20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/51932eng2046-206910.1039/C5RA19785Fhttp://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C5RA19785Finfo: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:RCAAP2023-07-21T12:34:36Zoai:repositorium.sdum.uminho.pt:1822/51932Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:30:18.896074Repositório 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 Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
title Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
spellingShingle Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
Marinho, Elina Margarida Ribeiro
2-(2-amino)quinazoline-4-amine
aromatic aldehydes
Ciências Naturais::Ciências Químicas
Science & Technology
title_short Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
title_full Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
title_fullStr Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
title_full_unstemmed Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
title_sort Acid catalyzed synthesis of 2-(2-aminophenyl)quinazoline-4-amine and reaction with aromatic aldehydes
author Marinho, Elina Margarida Ribeiro
author_facet Marinho, Elina Margarida Ribeiro
Proença, M. Fernanda R. P.
author_role author
author2 Proença, M. Fernanda R. P.
author2_role author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Marinho, Elina Margarida Ribeiro
Proença, M. Fernanda R. P.
dc.subject.por.fl_str_mv 2-(2-amino)quinazoline-4-amine
aromatic aldehydes
Ciências Naturais::Ciências Químicas
Science & Technology
topic 2-(2-amino)quinazoline-4-amine
aromatic aldehydes
Ciências Naturais::Ciências Químicas
Science & Technology
description 2-(2-Aminophenyl)quinazoline-4-amine, prepared from a quinazolino[3,4-a]quinazoline, were reacted with aromatic aldehydes under conventional heating or microwave irradiation, leading to high yields of tetracyclic dihydroquinazolines.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/51932
url http://hdl.handle.net/1822/51932
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2046-2069
10.1039/C5RA19785F
http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C5RA19785F
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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