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Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.provenance | CONICET | - |
dc.creator | Martins, Guilherme M. | - |
dc.creator | Zeni, Gilson | - |
dc.creator | Back, David F. | - |
dc.creator | Kaufman, Teodoro Saul | - |
dc.creator | Silveira, Claudio C. | - |
dc.date | 2016-06-06T21:06:12Z | - |
dc.date | 2016-06-06T21:06:12Z | - |
dc.date | 2015-10-12 | - |
dc.date | 2016-06-01T13:48:52Z | - |
dc.date.accessioned | 2019-04-29T15:36:18Z | - |
dc.date.available | 2019-04-29T15:36:18Z | - |
dc.date.issued | 2015-10-12 | - |
dc.identifier | Martins, 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.identifier | 1615-4150 | - |
dc.identifier | http://hdl.handle.net/11336/6063 | - |
dc.identifier.uri | http://rodna.bn.gov.ar:8080/jspui/handle/bnmm/297572 | - |
dc.description | A 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.description | Fil: Martins, Guilherme M.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil | - |
dc.description | Fil: Zeni, Gilson. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil | - |
dc.description | Fil: Back, David F.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil | - |
dc.description | Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina | - |
dc.description | Fil: Silveira, Claudio C.. Universidade Federal de Santa Maria. Departamento de Qu ímica; Brasil | - |
dc.format | application/pdf | - |
dc.format | application/pdf | - |
dc.language | eng | - |
dc.publisher | Wiley | - |
dc.relation | info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/adsc.201500275/abstract | - |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/adsc.201500275 | - |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/10.1002/adsc.201500275 | - |
dc.rights | info:eu-repo/semantics/restrictedAccess | - |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | - |
dc.source | reponame:CONICET Digital (CONICET) | - |
dc.source | instname:Consejo Nacional de Investigaciones Científicas y Técnicas | - |
dc.source | instacron:CONICET | - |
dc.source.uri | http://hdl.handle.net/11336/6063 | - |
dc.subject | 3H-benzo[e]indoles | - |
dc.subject | heterocycles | - |
dc.subject | iodocyclization | - |
dc.subject | phenylacetylenes | - |
dc.subject | Química Orgánica | - |
dc.subject | Ciencias Químicas | - |
dc.subject | CIENCIAS NATURALES Y EXACTAS | - |
dc.title | Expedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.type | info:ar-repo/semantics/articulo | - |
Aparece en las colecciones: | CONICET |
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