化学
电泳剂
卤化物
烷基
芳基
亲核细胞
选择性
催化作用
卤代芳基
组合化学
偶联反应
光化学
镍
有机化学
作者
Soumik Biswas,Daniel J. Weix
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.
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