Chiral Triphenylprolinol Ligands for the Efficient Catalytic Asymmetric Arylation of Aldehydes
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 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 |
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 |