Efficient Nickel Precatalysts for Suzuki-Miyaura Cross-Coupling of Aryl Chlorides and Arylboronic Acids Under Mild Conditions

被引:0
|
作者
John, Morgan E. [1 ]
Nutt, Michael J. [1 ]
Offer, Josephine E. [1 ]
Duczynski, Jeremy A. [1 ]
Yamazaki, Ken [2 ]
Miura, Tomoya [2 ]
Moggach, Stephen A. [1 ]
Koutsantonis, George A. [1 ]
Dorta, Reto [1 ]
Stewart, Scott G. [1 ]
机构
[1] Univ Western Australia, Sch Mol Sci, M310,35 Stirling Highway, Crawley, WA 6009, Australia
[2] Okayama Univ, Div Appl Chem, Tsushima, Okayama 7008530, Japan
基金
澳大利亚研究理事会;
关键词
Air Stable; Aryl Chlorides; Boronic Acids; Nickel Catalysis; Room Temperature; Suzuki-Miyaura Cross-Coupling; CATALYTIC C-C; COMPLEXES SYNTHESIS; BENZYL CHLORIDES; LIGATION STATE; PHOSPHINE; REACTIVITY; LIGANDS; HALIDES; NI(II); ELECTROPHILES;
D O I
10.1002/anie.202504108
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and catalytic properties of Ni(II) complexes with the general formula Ni(NHC)[P(OR)3](Ar)Cl are described. These complexes are air-stable and extremely effective precatalysts in the Suzuki-Miyaura cross-coupling reaction. The reaction protocols described allow for the cross-coupling of aryl chlorides and arylboronic acids, employing low catalytic loading, to deliver a large variety of functionalized biaryl compounds. For the coupling of aryl chlorides with N-heterocyclic boronic acids, TBAF was used as an additive to afford nitrogen-containing biaryl products. Overall, these reaction protocols operate at room or mild temperatures and can be applied to a variety of electronically and sterically differentiated coupling partners. Fundamental insights into the mechanism of this reaction, including the proposed formation of the catalytically active Ni(NHC)[P(Oi-Pr)3] and resting state species, are also reported.
引用
收藏
页数:11
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