Artículos de revistas
The first examples of the enantioselective Heck-Matsuda reaction: arylation of unactivated cyclic olefins using chiral bisoxazolines
Registro en:
Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 53, n. 26, n. 3325, n. 3328, 2012.
0040-4039
WOS:000304851500031
10.1016/j.tetlet.2012.04.079
Autor
Correia, CRD
Oliveira, CC
Salles, AG
Santos, EAF
Institución
Resumen
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Successful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96% isolated yields and in enantiomeric excesses of 54% up to 84%. (C) 2012 Elsevier Ltd. All rights reserved. 53 26 3325 3328 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)