Monooxychlorophosphine as a novel and efficient ligand for palladium-catalyzed suzuki-miyaura cross-coupling of aryl chlorides


Autoria(s): Mai WP; Lv GH; Gao LX
Data(s)

2007

Resumo

A new sterically hindered monooxychlorophosphine was synthesized and the complex generated in situ from its reaction with Pd-2(dba)(3) promoted the Suzuki-Miyaura reactions of arylboronic acids with aryl chlorides in good yields.

Identificador

http://ir.ciac.jl.cn/handle/322003/14369

http://www.irgrid.ac.cn/handle/1471x/150128

Idioma(s)

英语

Fonte

Mai WP;Lv GH;Gao LX.Monooxychlorophosphine as a novel and efficient ligand for palladium-catalyzed suzuki-miyaura cross-coupling of aryl chlorides,SYNLETT ,2007 ,(14):2247-2251

Palavras-Chave #HIGHLY-ACTIVE CATALYST #ARYLBORONIC ACIDS #MILD CONDITIONS #ALKYL BROMIDES #BORONIC ACIDS #HALIDES #PHOSPHINE #AMINATION #VANCOMYCIN #CONVENIENT
Tipo

期刊论文