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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.
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页数:11
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