Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles

Detalhes bibliográficos
Autor(a) principal: Pinho e Melo, Teresa M. V. D.
Data de Publicação: 2000
Outros Autores: Lopes, Cláudia S. J., Gonsalves, António M. d'A. Rocha
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5241
https://doi.org/10.1002/chin.200048131
Resumo: Nucleophilic substitution reactions of 2-halo-2H-azirine with potassium phthalimide and aniline allowed the preparation of new substituted 2H-azirines. The reactions of 2-bromo-3-phenyl-2H-azirine-2-carboxylate with methylamine led to the synthesis of [alpha]-diimines and from the reaction with water, a 3-oxazoline was obtained.
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spelling Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles2H-azirines[alpha]-diimines3-oxazolineNucleophilic substitution reactions of 2-halo-2H-azirine with potassium phthalimide and aniline allowed the preparation of new substituted 2H-azirines. The reactions of 2-bromo-3-phenyl-2H-azirine-2-carboxylate with methylamine led to the synthesis of [alpha]-diimines and from the reaction with water, a 3-oxazoline was obtained.http://www.sciencedirect.com/science/article/B6THS-4152YMR-K/1/e94005b66b66b6820ad27458f2562edd2000info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5241http://hdl.handle.net/10316/5241https://doi.org/10.1002/chin.200048131engTetrahedron Letters. 41:37 (2000) 7217-7220Pinho e Melo, Teresa M. V. D.Lopes, Cláudia S. J.Gonsalves, António M. d'A. Rochainfo: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:RCAAP2020-11-06T16:48:35Zoai:estudogeral.uc.pt:10316/5241Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:22.870611Repositório 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 and reactivity of 2-halo-2H-azirines towards nucleophiles
title Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
spellingShingle Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
Pinho e Melo, Teresa M. V. D.
2H-azirines
[alpha]-diimines
3-oxazoline
title_short Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
title_full Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
title_fullStr Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
title_full_unstemmed Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
title_sort Synthesis and reactivity of 2-halo-2H-azirines towards nucleophiles
author Pinho e Melo, Teresa M. V. D.
author_facet Pinho e Melo, Teresa M. V. D.
Lopes, Cláudia S. J.
Gonsalves, António M. d'A. Rocha
author_role author
author2 Lopes, Cláudia S. J.
Gonsalves, António M. d'A. Rocha
author2_role author
author
dc.contributor.author.fl_str_mv Pinho e Melo, Teresa M. V. D.
Lopes, Cláudia S. J.
Gonsalves, António M. d'A. Rocha
dc.subject.por.fl_str_mv 2H-azirines
[alpha]-diimines
3-oxazoline
topic 2H-azirines
[alpha]-diimines
3-oxazoline
description Nucleophilic substitution reactions of 2-halo-2H-azirine with potassium phthalimide and aniline allowed the preparation of new substituted 2H-azirines. The reactions of 2-bromo-3-phenyl-2H-azirine-2-carboxylate with methylamine led to the synthesis of [alpha]-diimines and from the reaction with water, a 3-oxazoline was obtained.
publishDate 2000
dc.date.none.fl_str_mv 2000
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/10316/5241
http://hdl.handle.net/10316/5241
https://doi.org/10.1002/chin.200048131
url http://hdl.handle.net/10316/5241
https://doi.org/10.1002/chin.200048131
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Tetrahedron Letters. 41:37 (2000) 7217-7220
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv aplication/PDF
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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
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