Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid


Autoria(s): SINGH, Fateh V.; MILAGRE, Humberto M. S.; BERLIN, Mafcos N.; STEFANI, Helio A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

The oxidation of geminal biaryl ethenes 3 and 1,3-enynes 5 using m-chloroperbenzoic acid in dichloromethane at room temperature presents a catalyst-free approach for the synthesis of functionalized benzophenones 4 and ynones 6, respectively. (C) 2009 Elsevier Ltd. All rights reserved.

FAPESP[07/59404-2]

FAPESP[07/514669]

CNPq[300613/2007-5]

Identificador

TETRAHEDRON LETTERS, v.50, n.20, p.2312-2316, 2009

0040-4039

http://producao.usp.br/handle/BDPI/19694

10.1016/j.tetlet.2009.02.164

http://dx.doi.org/10.1016/j.tetlet.2009.02.164

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Tetrahedron Letters

Direitos

closedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #CROSS-COUPLING REACTION #ELECTROSPRAY-IONIZATION MASS #ACYL CHLORIDES #ARYLBORONIC ACIDS #SELECTIVE OXIDATION #GARCINIA-MULTIFLORA #NATURAL-PRODUCTS #DOUBLE-BOND #ALCOHOLS #MECHANISM #Chemistry, Organic
Tipo

article

original article

publishedVersion