[Pd(C∧N)(X)(PPh3)] palladacycles react with 2,4,6-trifluorophenyl boronic acid to give stable transmetallation products of the type [Pd(C∧N)(2,4,6-F3C6H2)(PPh3)]

被引:23
|
作者
Kapdi, Anant R. [1 ]
Dhangar, Gopal [1 ]
Luis Serrano, Jose [2 ]
Perez, Jose [2 ]
Garcia, Luis [2 ]
Fairlamb, Ian J. S. [3 ]
机构
[1] Inst Chem Technol, Dept Chem, Bombay 400019, Maharashtra, India
[2] Univ Politecn Cartagena, Dept Ingn Minera Geol & Cartog, Area Quim Inorgon, Cartagena 30203, Spain
[3] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
SUZUKI-MIYAURA REACTIONS; COUPLING REACTIONS; RECYCLABLE CATALYSTS; PALLADIUM; COMPLEXES; ARYL; PD(OAC)(2); LIGANDS; BASE;
D O I
10.1039/c4cc04203d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct transmetallation between palladacyclic complexes and arylboronic acid occurs to give isolable transmetallation products. In THF, the reaction occurs <0.5 h. Prolonged reaction leads to the generation of a dinuclear Pd complex bearing bridging It-hydroxo and mu-acetoxy ligands. Insight into precatalyst activation for Suzuki-Miyaura cross-couplings mediated by palladacycles has been gained, where acetate and N-imidate anions activate a neutral arylboronic acid.
引用
收藏
页码:9859 / 9861
页数:3
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