Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/105741
Type: Artigo de periódico
Title: 1,5-asymmetric Induction In Boron-mediated Aldol Reactions Of β-alkoxy Methylketones
Author: Dias L.C.
De Marchi A.A.
Ferreira M.A.B.
Aguilar A.M.
Abstract: (Chemical Equation Presented) Good levels of substrate-controlled, 1,5-syn-stereoinduction are obtained in boron-mediated aldol reactions of β-trichloromethyl-β-alkoxy and β-trifluoromethyl-β-alkoxy methylketones with achiral aldehydes, independent of the nature of the β-alkoxy protecting group (TBS or PMB). In the case of boron aldol reactions of β-aryl-β-alkoxy methylketones, the 1,5-anti-adducts were obtained with high levels of diastereoselectivity only with a β-OPMB group. © 2008 American Chemical Society.
Editor: 
Citation: Journal Of Organic Chemistry. , v. 73, n. 16, p. 6299 - 6311, 2008.
Rights: fechado
Identifier DOI: 10.1021/jo8009165
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-50149104770&partnerID=40&md5=7025b39feec95587f900766a5e608f7f
Date Issue: 2008
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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