dc.creatorRodrigues, MT
dc.creatorSantos, MS
dc.creatorSantos, H
dc.creatorCoelho, F
dc.date2014
dc.date36892
dc.date2014-07-30T13:38:38Z
dc.date2015-11-26T17:47:40Z
dc.date2014-07-30T13:38:38Z
dc.date2015-11-26T17:47:40Z
dc.date.accessioned2018-03-29T00:30:22Z
dc.date.available2018-03-29T00:30:22Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 55, n. 1, n. 180, n. 183, 2014.
dc.identifier0040-4039
dc.identifierWOS:000329960500038
dc.identifier10.1016/j.tetlet.2013.10.146
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/52473
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/52473
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1288853
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionIn 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.description55
dc.description1
dc.description180
dc.description183
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectImidazole
dc.subjectMorita-Baylis-Hillman
dc.subjectMichael reaction
dc.subjectDiastereoselective
dc.subjectIonic liquids
dc.subjectThiazole Alkaloids
dc.subjectAntifungal Agents
dc.subjectHeterocycles
dc.subjectEnantiomers
dc.subjectChemistry
dc.subjectOxazole
dc.subjectAcid
dc.title1,1 '-Carbonyldiimidazole mediates the synthesis of N-substituted imidazole derivatives from Morita-Baylis-Hillman adducts
dc.typeArtículos de revistas


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