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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Jiménez Montejo, Fabiola Eloísa | - |
dc.date.accessioned | 2013-02-26T18:20:49Z | - |
dc.date.available | 2013-02-26T18:20:49Z | - |
dc.date.issued | 2013-02-26 | - |
dc.identifier.uri | http://www.repositoriodigital.ipn.mx/handle/123456789/13810 | - |
dc.description | Article | es |
dc.description.abstract | An efficient synthetic approach to the substituted benzo[b]furan and benzo[b]thiophene scaffolds by iodine-mediated cyclization of the corresponding enaminones is described. This protocol was applied to a large series of these latter precursors to afford the respective benzoheterocycles substituted at the C-2 position by a carbonyl group functionality. A study of the factors that control this process reveals that the reactivity depends on the presence of electron-donor groups in the aryl ring of the aryloxycarbonylic and arylthiocarbonylic moieties. | es |
dc.description.sponsorship | Instituto Politécnico Nacional CIBA-Tlaxcala | es |
dc.subject | Enaminones | es |
dc.title | Efficient Synthetic Approach to Substituted Benzo[b]furans and Benzo[b]thiophenes by Iodine-Promoted Cyclization of Enaminones | es |
dc.type | Article | es |
dc.description.especialidad | Medico-Biológicas | es |
dc.description.tipo | es | |
Aparece en las colecciones: | Congresos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
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1. JHET 2012 (impresion).pdf | 71.9 kB | Adobe PDF | Visualizar/Abrir |
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