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dc.provenanceCONICET-
dc.creatorMartins, Guilherme M.-
dc.creatorZeni, Gilson-
dc.creatorBack, David F.-
dc.creatorKaufman, Teodoro Saul-
dc.creatorSilveira, Claudio C.-
dc.date2016-06-06T21:06:12Z-
dc.date2016-06-06T21:06:12Z-
dc.date2015-10-12-
dc.date2016-06-01T13:48:52Z-
dc.date.accessioned2019-04-29T15:36:18Z-
dc.date.available2019-04-29T15:36:18Z-
dc.date.issued2015-10-12-
dc.identifierMartins, Guilherme M.; Zeni, Gilson; Back, David F.; Kaufman, Teodoro Saul; Silveira, Claudio C.; Expedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles; Wiley; Advanced Synthesis & Catalysis (print); 357; 14-15; 12-10-2015; 3255-3261-
dc.identifier1615-4150-
dc.identifierhttp://hdl.handle.net/11336/6063-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/297572-
dc.descriptionA facile and expedient iodocyclization of 4-(2-prop-1-ynylphenyl)-1H-pyrroles towards the synthesis of polysubstituted 3H-benzo[e]indoles is reported. The transformation was optimized and the best results were obtained by using iodine (1.2 equiv,) in dichloromethane, and potassium carbonate as base. The starting 1,2,3,4-tetrasubstituted pyrroles were efficiently obtained by means of a nickel(II) chloride-promoted four-component (nitromethane, amine, 2-alkynylbenzaldehyde and ethyl acetoacetate) reaction. Further functionalization of the resulting 5-iodoheterocycles was also explored.-
dc.descriptionFil: Martins, Guilherme M.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil-
dc.descriptionFil: Zeni, Gilson. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil-
dc.descriptionFil: Back, David F.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil-
dc.descriptionFil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina-
dc.descriptionFil: Silveira, Claudio C.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherWiley-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/adsc.201500275/abstract-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/adsc.201500275-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/10.1002/adsc.201500275-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/6063-
dc.subject3H-benzo[e]indoles-
dc.subjectheterocycles-
dc.subjectiodocyclization-
dc.subjectphenylacetylenes-
dc.subjectQuímica Orgánica-
dc.subjectCiencias Químicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleExpedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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