2H-Azirines as dipolarophiles

Detalhes bibliográficos
Autor(a) principal: Melo, Teresa M. V. D. Pinho e
Data de Publicação: 2003
Outros Autores: Cardoso, Ana L., Gomes, Clara S. B., 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/10316/5158
https://doi.org/10.1016/S0040-4039(03)01534-X
Resumo: 2H-Azirine-3-carboxylates unsubstituted at C-2 act as dipolarophiles in the reaction with diazomethane giving new 4,5-dihydro-3H-pyrazole derivatives. The synthesis of a pyrimidine was also achieved via 1,3-dipolar cycloaddition of methyl 2-bromo-3-phenyl-2H-azirine-2-carboxylate with an azomethine ylide.
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spelling 2H-Azirines as dipolarophiles2H-azirines1,3-dipolar cycloaddition3H-pyrazolepyrimidine2H-Azirine-3-carboxylates unsubstituted at C-2 act as dipolarophiles in the reaction with diazomethane giving new 4,5-dihydro-3H-pyrazole derivatives. The synthesis of a pyrimidine was also achieved via 1,3-dipolar cycloaddition of methyl 2-bromo-3-phenyl-2H-azirine-2-carboxylate with an azomethine ylide.http://www.sciencedirect.com/science/article/B6THS-493P1M1-17/1/5df1370edad7138f3cae89fadd9b5c4d2003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5158http://hdl.handle.net/10316/5158https://doi.org/10.1016/S0040-4039(03)01534-XengTetrahedron Letters. 44:33 (2003) 6313-6315Melo, Teresa M. V. D. Pinho eCardoso, Ana L.Gomes, Clara S. B.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:RCAAP2021-09-02T11:07:48Zoai:estudogeral.uc.pt:10316/5158Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:35.726725Repositório 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 2H-Azirines as dipolarophiles
title 2H-Azirines as dipolarophiles
spellingShingle 2H-Azirines as dipolarophiles
Melo, Teresa M. V. D. Pinho e
2H-azirines
1,3-dipolar cycloaddition
3H-pyrazole
pyrimidine
title_short 2H-Azirines as dipolarophiles
title_full 2H-Azirines as dipolarophiles
title_fullStr 2H-Azirines as dipolarophiles
title_full_unstemmed 2H-Azirines as dipolarophiles
title_sort 2H-Azirines as dipolarophiles
author Melo, Teresa M. V. D. Pinho e
author_facet Melo, Teresa M. V. D. Pinho e
Cardoso, Ana L.
Gomes, Clara S. B.
Gonsalves, António M. d'A. Rocha
author_role author
author2 Cardoso, Ana L.
Gomes, Clara S. B.
Gonsalves, António M. d'A. Rocha
author2_role author
author
author
dc.contributor.author.fl_str_mv Melo, Teresa M. V. D. Pinho e
Cardoso, Ana L.
Gomes, Clara S. B.
Gonsalves, António M. d'A. Rocha
dc.subject.por.fl_str_mv 2H-azirines
1,3-dipolar cycloaddition
3H-pyrazole
pyrimidine
topic 2H-azirines
1,3-dipolar cycloaddition
3H-pyrazole
pyrimidine
description 2H-Azirine-3-carboxylates unsubstituted at C-2 act as dipolarophiles in the reaction with diazomethane giving new 4,5-dihydro-3H-pyrazole derivatives. The synthesis of a pyrimidine was also achieved via 1,3-dipolar cycloaddition of methyl 2-bromo-3-phenyl-2H-azirine-2-carboxylate with an azomethine ylide.
publishDate 2003
dc.date.none.fl_str_mv 2003
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/10316/5158
http://hdl.handle.net/10316/5158
https://doi.org/10.1016/S0040-4039(03)01534-X
url http://hdl.handle.net/10316/5158
https://doi.org/10.1016/S0040-4039(03)01534-X
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Tetrahedron Letters. 44:33 (2003) 6313-6315
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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