Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/64732
Type: Artigo de periódico
Title: Enantioselective total synthesis of (-)-ericanone
Author: Dias, LC
Kuroishi, PK
Polo, EC
de Lucca, EC
Abstract: The first total synthesis of (-)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti aldol reaction to install the hydroxyl group at C7. (C) 2012 Elsevier Ltd. All rights reserved.
Subject: Total synthesis
Natural product
(-)-Ericanone
Aldol reaction
Boron enolate
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.tetlet.2012.12.033
Date Issue: 2013
Appears in Collections:Unicamp - Artigos e Outros Documentos

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