One-pot synthesis of alpha,beta-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols


Autoria(s): SINGH, Fateh V.; PENA, Jesus M.; STEFANI, Helio A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

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

http://dx.doi.org/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