Catalytic Enantioselective alpha-Arylation of Carbonyl Compounds
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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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 |
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 |