Enantioselective Arylations Catalyzed by Carbohydrate-Based Chiral Amino Alcohols
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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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 |
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 |