Mechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl Halides

被引:502
|
作者
Biswas, Soumik [1 ]
Weix, Daniel J. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
关键词
FUNCTIONALIZED GRIGNARD-REAGENTS; REDUCTIVE CONJUGATE ADDITION; CARBON BOND FORMATION; OXIDATIVE ADDITION; RADICAL CATALYSIS; ORGANIC HALIDES; AROMATIC HALIDES; KETONE FORMATION; DIRECT ARYLATION; COMPLEXES;
D O I
10.1021/ja407589e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl halide, offers many advantages over conventional cross-coupling methods that require a carbon nucleophile. Despite its promise as a versatile synthetic strategy, a limited understanding of the mechanism and origin of cross selectivity has hindered progress in reaction development and design. Herein, we shed light on the mechanism for the nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides and demonstrate that the selectivity arises from an unusual catalytic cycle that combines both polar and radical steps to form the new C-C bond.
引用
收藏
页码:16192 / 16197
页数:6
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