One-pot synthesis of alpha,beta-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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Resumo |
Described herein is a one-pot synthesis of a,p-epoxy ketones using a palladium-catalyzed epoxidation-oxidation sequence. Functionalized terminal allylic alcohols are treated with m-CPBA Under mild reaction conditions to obtain the alpha,beta-epoxy ketones. The main benefit of this approach is that the epoxidation of the terminal double bond and the oxidation of the secondary alcohol occured in the same reaction under mild reactions and both electron-donating and electron-withdrawing functionalities are tolerated in the reaction sequence. (C) 2010 Elsevier Ltd. All rights reserved. FAPESP[07/59404-2] FAPESP[07/51466-9] CNPq[300.613/2007-5] |
Identificador |
TETRAHEDRON LETTERS, v.51, n.13, p.1671-1673, 2010 0040-4039 http://producao.usp.br/handle/BDPI/19845 10.1016/j.tetlet.2010.01.065 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD |
Relação |
Tetrahedron Letters |
Direitos |
closedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #ACYCLIC CONJUGATED DIENES #REACTIVITY #EPOXIDES #Chemistry, Organic |
Tipo |
article original article publishedVersion |