Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/68282
Type: Artigo de periódico
Title: Heterocycles from Morita-Baylis-Hillman adducts: synthesis of 5-oxopyrazolidines, arylidene-5-oxopyrazolidines, and oxo-2,5-dihydro-pyrazols
Author: Correia, JTM
Rodrigues, MT
Santos, H
Tormena, CF
Coelho, F
Abstract: Starting from Morita-Baylis-Hillman (MBH) adducts, an approach for the synthesis of oxopyrazolidines, arylidene-oxopyrazolidines, and oxo-2,5-dihydropyrazoles is described. The method is based on a tandem process involving a Michael addition of amino-guanidine into silylated and acetylated MBH adducts, followed by intramolecular cyclization. The use of acetylated MBH adducts led also to the synthesis of unusual pyrazoles, which is facilitated by an unexpected base-mediated equilibrium. (c) 2012 Elsevier Ltd. All rights reserved.
Subject: Morita-Baylis-Hillman
Pyrazolones
Pyrazolidines
Michael reaction
Heterocycles
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.tet.2012.10.057
Date Issue: 2013
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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