New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones

Detalhes bibliográficos
Autor(a) principal: Cunha, Silvio do Desterro
Data de Publicação: 2007
Outros Autores: Damasceno, Fabiano, Ferrari, Jailton
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFBA
Texto Completo: http://repositorio.ufba.br/ri/handle/ri/14401
Resumo: Texto completo: acesso restrito. p. 469-474
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spelling Cunha, Silvio do DesterroDamasceno, FabianoFerrari, JailtonCunha, Silvio do DesterroDamasceno, FabianoFerrari, Jailton2014-01-21T11:57:21Z20070040-4039http://repositorio.ufba.br/ri/handle/ri/14401v. 48, n. 33Texto completo: acesso restrito. p. 469-474The formal aza-[3+2] cycloaddition reactions of cyclopropenones and cyclic enaminones, including a chiral one, were employed for the first time in the direct formation of new pyrrolidine and indolizidine derivatives. The regiochemistry of cyclization is dependent of both ring size and steric factors of enaminones.Submitted by Suelen Reis (suziy.ellen@gmail.com) on 2014-01-21T11:57:21Z No. of bitstreams: 1 1-s2.0-S0040403907012014-main.pdf: 164117 bytes, checksum: 4d792e08d21818021c978fafaa17666d (MD5)Made available in DSpace on 2014-01-21T11:57:21Z (GMT). No. of bitstreams: 1 1-s2.0-S0040403907012014-main.pdf: 164117 bytes, checksum: 4d792e08d21818021c978fafaa17666d (MD5) Previous issue date: 2007http://dx.doi.org/10.1016/j.tetlet.2007.06.087reponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAEnaminonePyrrolizidineIndolizidineNew alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenonesTetrahedron Lettersinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10000-01-01info:eu-repo/semantics/openAccessengORIGINAL1-s2.0-S0040403907012014-main.pdf1-s2.0-S0040403907012014-main.pdfapplication/pdf164117https://repositorio.ufba.br/bitstream/ri/14401/1/1-s2.0-S0040403907012014-main.pdf4d792e08d21818021c978fafaa17666dMD51LICENSElicense.txtlicense.txttext/plain1345https://repositorio.ufba.br/bitstream/ri/14401/2/license.txtff6eaa8b858ea317fded99f125f5fcd0MD52TEXT1-s2.0-S0040403907012014-main.pdf.txt1-s2.0-S0040403907012014-main.pdf.txtExtracted texttext/plain14431https://repositorio.ufba.br/bitstream/ri/14401/3/1-s2.0-S0040403907012014-main.pdf.txta1a05a04213353418adaea47e8e3da0bMD53ri/144012022-07-05 14:04:17.857oai:repositorio.ufba.br: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Repositório InstitucionalPUBhttp://192.188.11.11:8080/oai/requestopendoar:19322022-07-05T17:04:17Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA)false
dc.title.pt_BR.fl_str_mv New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
dc.title.alternative.pt_BR.fl_str_mv Tetrahedron Letters
title New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
spellingShingle New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
Cunha, Silvio do Desterro
Enaminone
Pyrrolizidine
Indolizidine
title_short New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
title_full New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
title_fullStr New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
title_full_unstemmed New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
title_sort New alkaloid-like heterocycles via formal aza-[3+2] cycloaddition reaction of cyclic enaminones with cyclopropenones
author Cunha, Silvio do Desterro
author_facet Cunha, Silvio do Desterro
Damasceno, Fabiano
Ferrari, Jailton
author_role author
author2 Damasceno, Fabiano
Ferrari, Jailton
author2_role author
author
dc.contributor.author.fl_str_mv Cunha, Silvio do Desterro
Damasceno, Fabiano
Ferrari, Jailton
Cunha, Silvio do Desterro
Damasceno, Fabiano
Ferrari, Jailton
dc.subject.por.fl_str_mv Enaminone
Pyrrolizidine
Indolizidine
topic Enaminone
Pyrrolizidine
Indolizidine
description Texto completo: acesso restrito. p. 469-474
publishDate 2007
dc.date.issued.fl_str_mv 2007
dc.date.accessioned.fl_str_mv 2014-01-21T11:57:21Z
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://repositorio.ufba.br/ri/handle/ri/14401
dc.identifier.issn.none.fl_str_mv 0040-4039
dc.identifier.number.pt_BR.fl_str_mv v. 48, n. 33
identifier_str_mv 0040-4039
v. 48, n. 33
url http://repositorio.ufba.br/ri/handle/ri/14401
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.pt_BR.fl_str_mv http://dx.doi.org/10.1016/j.tetlet.2007.06.087
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFBA
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