Enantioselective Arylations Catalyzed by Carbohydrate-Based Chiral Amino Alcohols


Autoria(s): WOUTERS, Ana Dioneia; TROSSINI, Gustavo H. G.; STEFANI, Helio A.; LUDTKE, Diogo S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

The application of carbohydrate-derived amino alcohols in the asymmetric arylation of aldehydes by using arylboronic acids as the source of transferable aryl groups is described. The best ligand is derived from the readily available sugar D-xylose and it mediates the addition of a range of arylboronic acids to various aromatic aldehydes in excellent yields and high enantiomeric excesses.

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

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Comissao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Identificador

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, n.12, p.2351-2356, 2010

1434-193X

http://producao.usp.br/handle/BDPI/19668

10.1002/ejoc.201000113

http://dx.doi.org/10.1002/ejoc.201000113

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

European Journal of Organic Chemistry

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #Arylation #Boron #Zinc #Carbohydrates #Asymmetric catalysis #ASYMMETRIC ARYL TRANSFER #PHENYL TRANSFER #ORGANOZINC REAGENTS #BORONIC ACIDS #ALDEHYDES #LIGANDS #DERIVATIVES #ADDITIONS #DIARYLMETHANOLS #DIETHYLZINC #Chemistry, Organic
Tipo

article

original article

publishedVersion