Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/52473
Type: Artigo de periódico
Title: 1,1 '-Carbonyldiimidazole mediates the synthesis of N-substituted imidazole derivatives from Morita-Baylis-Hillman adducts
Author: Rodrigues, MT
Santos, MS
Santos, H
Coelho, F
Abstract: 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.
Subject: Imidazole
Morita-Baylis-Hillman
Michael reaction
Diastereoselective
Ionic liquids
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Citationo: Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 55, n. 1, n. 180, n. 183, 2014.
Rights: fechado
Identifier DOI: 10.1016/j.tetlet.2013.10.146
Date Issue: 2014
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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