Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach


Autoria(s): BELLOMO, Ana; GONZALEZ, David; STEFANI, Helio A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

The Suzuki-Miyaura cross-coupling reaction of a hydroxylated vinyl bromide obtained by a chemoenzymatic approach with a diverse range of potassium organotrifluoroborates has been accomplished catalyzed by Pd(PPh(3))(4) in satisfactory yields. A variety of functional groups are tolerated in the nucleophilic partner. (C) 2008 Elsevier B.V. All rights reserved.

Identificador

JOURNAL OF ORGANOMETALLIC CHEMISTRY, v.693, n.6, p.1136-1142, 2008

0022-328X

http://producao.usp.br/handle/BDPI/19728

10.1016/j.jorganchem.2008.01.006

http://dx.doi.org/10.1016/j.jorganchem.2008.01.006

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE SA

Relação

Journal of Organometallic Chemistry

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE SA

Palavras-Chave #Suzuki-Miyaura cross-coupling reaction #potassium organotrifluoroborate salts #conduritol nucleus #biocatalysis #CROSS-COUPLING REACTIONS #CHEMOENZYMATIC SYNTHESIS #EFFICIENT SYNTHESIS #VINYLIC TELLURIDES #ALKENYL BROMIDES #NATURAL-PRODUCTS #CHEMISTRY #ARYL #SALTS #ACIDS #Chemistry, Inorganic & Nuclear #Chemistry, Organic
Tipo

article

original article

publishedVersion