dc.creator | Rodrigues, MT | |
dc.creator | Santos, MS | |
dc.creator | Santos, H | |
dc.creator | Coelho, F | |
dc.date | 2014 | |
dc.date | 36892 | |
dc.date | 2014-07-30T13:38:38Z | |
dc.date | 2015-11-26T17:47:40Z | |
dc.date | 2014-07-30T13:38:38Z | |
dc.date | 2015-11-26T17:47:40Z | |
dc.date.accessioned | 2018-03-29T00:30:22Z | |
dc.date.available | 2018-03-29T00:30:22Z | |
dc.identifier | Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 55, n. 1, n. 180, n. 183, 2014. | |
dc.identifier | 0040-4039 | |
dc.identifier | WOS:000329960500038 | |
dc.identifier | 10.1016/j.tetlet.2013.10.146 | |
dc.identifier | http://www.repositorio.unicamp.br/jspui/handle/REPOSIP/52473 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/52473 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1288853 | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | In this Letter, we describe a simple and straightforward method for the synthesis of N-substituted imidazole derivatives. 1,1-carbonyldiimidazole mediates the process, which requires no activation group step. We obtained imidazole derivatives in high yields and with short reaction times. To demonstrate the synthetic significance of the aforementioned compounds, we also describe the synthesis of novel ionic liquids from these derivatives. (C) 2013 Elsevier Ltd. All rights reserved. | |
dc.description | 55 | |
dc.description | 1 | |
dc.description | 180 | |
dc.description | 183 | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.language | en | |
dc.publisher | Pergamon-elsevier Science Ltd | |
dc.publisher | Oxford | |
dc.publisher | Inglaterra | |
dc.relation | Tetrahedron Letters | |
dc.relation | Tetrahedron Lett. | |
dc.rights | fechado | |
dc.rights | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dc.source | Web of Science | |
dc.subject | Imidazole | |
dc.subject | Morita-Baylis-Hillman | |
dc.subject | Michael reaction | |
dc.subject | Diastereoselective | |
dc.subject | Ionic liquids | |
dc.subject | Thiazole Alkaloids | |
dc.subject | Antifungal Agents | |
dc.subject | Heterocycles | |
dc.subject | Enantiomers | |
dc.subject | Chemistry | |
dc.subject | Oxazole | |
dc.subject | Acid | |
dc.title | 1,1 '-Carbonyldiimidazole mediates the synthesis of N-substituted imidazole derivatives from Morita-Baylis-Hillman adducts | |
dc.type | Artículos de revistas | |