Catalytic Enantioselective alpha-Arylation of Carbonyl Compounds


Autoria(s): BURTOLOSO, Antonio C. B.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Enantioselective creation of benzylic quaternary centers still is a continuous challenge to many synthetic organic chemists. Among the existing methods for installation of this type of center, the direct asymmetric alpha-arylation of carbonyl compounds is very attractive due to the ready availability of the coupling substrates. Herein, we present some new tools to the catalytic asymmetric alpha-arylation of carbonyl compounds that overcame many of the drawbacks posted in previous methods for this type of reaction.

Identificador

SYNLETT, n.2, p.320-327, 2009

0936-5214

http://producao.usp.br/handle/BDPI/31586

10.1055/s-0028-1087673

http://dx.doi.org/10.1055/s-0028-1087673

Idioma(s)

eng

Publicador

GEORG THIEME VERLAG KG

Relação

Synlett

Direitos

restrictedAccess

Copyright GEORG THIEME VERLAG KG

Palavras-Chave #enolates #alpha-arylation #carbonyl compounds #palladium #nickel #quaternary benzylic centers #QUATERNARY STEREOCENTERS #ASYMMETRIC ARYLATION #RATE ACCELERATION #CARBENE LIGANDS #PALLADIUM #CONSTRUCTION #KETONES #NICKEL #COMPLEXES #ALDEHYDES #Chemistry, Organic
Tipo

article

original article

publishedVersion