Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/63358
Type: Artigo de periódico
Title: Najera oxime-derived palladacycles catalyze intermolecular Heck reaction with Morita-Baylis-Hillman adducts. An improved and highly efficient synthesis of alpha-benzyl-beta-ketoesters
Author: Ferreira, BRV
Pirovani, RV
Souza, LG
Coelho, F
Abstract: An improved and highly efficient synthesis of several alpha-benzyl-beta-ketoesters from Morita-Baylis-Hillman adducts is described. These adducts were used as substrates for an intermolecular Heck reaction catalyzed by a Najera oxime-derived palladacycles. These efficient catalytic conditions probed to be very selective providing only the corresponding functionalized beta-ketoesters in high yield with no decarboxylation product. It seems that the method herein described is one of the most efficient for the synthesis of alpha-benzyl-beta-ketoesters. (C) 2009 Elsevier Ltd. All rights reserved.
Subject: C-C bond formation
Heck reaction
Morita-Baylis-Hillman reaction
Palladacycles
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.tet.2009.06.084
Date Issue: 2009
Appears in Collections:Unicamp - Artigos e Outros Documentos

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