Chiral Triphenylprolinol Ligands for the Efficient Catalytic Asymmetric Arylation of Aldehydes


Autoria(s): MORO, Angelica Venturini; TIEKINK, Edward R. T.; ZUKERMAN-SCHPECTOR, Julio; LUEDTKE, Diogo S.; CORREIA, Carlos Roque D.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

The synthesis of new chiral amino alcohols by Heck arylation of an enecarbamate is described. These compounds were used as chiral ligands for the catalytic asymmetric arylation of aldehydes and can be easily recovered. Chiral, nonracemic diarylmethanols were obtained in high yields and enantioselectivities.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Identificador

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, n.19, p.3696-3703, 2010

1434-193X

http://producao.usp.br/handle/BDPI/19664

10.1002/ejoc.201000336

http://dx.doi.org/10.1002/ejoc.201000336

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

European Journal of Organic Chemistry

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #Asymmetric synthesis #Amino alcohols #Heck reaction #Chirality #Aldehydes #ARYL TRANSFER-REACTIONS #HIGHLY ENANTIOSELECTIVE ADDITION #ORGANOZINC REAGENTS #HECK ARYLATION #BORONIC ACIDS #ARENEDIAZONIUM SALTS #DIAZONIUM SALTS #TERTIARY ALCOHOLS #METHYL-ESTER #DERIVATIVES #Chemistry, Organic
Tipo

article

original article

publishedVersion