Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole

Detalhes bibliográficos
Autor(a) principal: Campos, Ana M. F. Oliveira
Data de Publicação: 2004
Outros Autores: Gonçalves, M. Sameiro T., Rodrigues, Lígia M., Proença, M. Fernanda R. P., Griffiths, John, Maia, Hernâni L. S., Kaja, Martin, Hrdina, Radim
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/1246
Resumo: Diazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.
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spelling Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazolePyrazoleDicyanopyrazoleScience & TechnologyDiazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.Junta Nacional de Investigação Científica e Tecnológica (IBQFUM); PRAXIS XXI - 2/2.1/QUI/44/94, BD-2566-93-RM; Socrates Programme.Science Reviews 2000 LtdUniversidade do MinhoCampos, Ana M. F. OliveiraGonçalves, M. Sameiro T.Rodrigues, Lígia M.Proença, M. Fernanda R. P.Griffiths, JohnMaia, Hernâni L. S.Kaja, MartinHrdina, Radim2004-022004-02-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/1246eng"Journal of Chemical Research". (2004) 115-117.0308-2342info: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:RCAAP2023-07-21T12:35:27ZPortal AgregadorONG
dc.title.none.fl_str_mv Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
title Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
spellingShingle Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
Campos, Ana M. F. Oliveira
Pyrazole
Dicyanopyrazole
Science & Technology
title_short Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
title_full Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
title_fullStr Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
title_full_unstemmed Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
title_sort Synthesis of novel derivatives of 4-amino-3,5-dicyanopyrazole
author Campos, Ana M. F. Oliveira
author_facet Campos, Ana M. F. Oliveira
Gonçalves, M. Sameiro T.
Rodrigues, Lígia M.
Proença, M. Fernanda R. P.
Griffiths, John
Maia, Hernâni L. S.
Kaja, Martin
Hrdina, Radim
author_role author
author2 Gonçalves, M. Sameiro T.
Rodrigues, Lígia M.
Proença, M. Fernanda R. P.
Griffiths, John
Maia, Hernâni L. S.
Kaja, Martin
Hrdina, Radim
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Campos, Ana M. F. Oliveira
Gonçalves, M. Sameiro T.
Rodrigues, Lígia M.
Proença, M. Fernanda R. P.
Griffiths, John
Maia, Hernâni L. S.
Kaja, Martin
Hrdina, Radim
dc.subject.por.fl_str_mv Pyrazole
Dicyanopyrazole
Science & Technology
topic Pyrazole
Dicyanopyrazole
Science & Technology
description Diazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.
publishDate 2004
dc.date.none.fl_str_mv 2004-02
2004-02-01T00:00:00Z
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/1822/1246
url http://hdl.handle.net/1822/1246
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv "Journal of Chemical Research". (2004) 115-117.
0308-2342
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 Science Reviews 2000 Ltd
publisher.none.fl_str_mv Science Reviews 2000 Ltd
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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