烷基
化学
催化作用
质子化
镍
循环伏安法
氧化还原
基质(水族馆)
结合
催化循环
组合化学
有机化学
激进的
烷基化
药物化学
阳极
高分子化学
电化学
分子
有机合成
电偶阳极
作者
Jing Zhang,Youliang He,Ping Fang,H. Xu,Tian‐Sheng Mei
摘要
We report a nickel-catalyzed electroreductive Giese hydroalkylation of unactivated tertiary alkyl bromides with electron-deficient alkenes. The transformation proceeds under mild, constant-current conditions in a simple undivided cell, employing an iron sacrificial anode and an accessible nickel/bipyridine catalyst system. This protocol features broad substrate scope, excellent functional-group tolerance, and high efficiency, enabling the late-stage modification of structurally complex molecules and pharmaceuticals. Mechanistic investigations-including cyclic voltammetry and deuterium-labeling experiments-indicate that the reaction operates through a Ni(I)/Ni(II) redox cycle that mediates single-electron activation of tertiary alkyl bromides. The resulting alkyl radicals undergo conjugate addition to electron-deficient alkenes, followed by cathodic reduction and protonation to furnish the hydroalkylation products.
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