化学
硼氢化
区域选择性
卡宾
硼烷
亲核细胞
有机化学
光催化
有机硼化合物
激进的
胺化
光化学
密度泛函理论
亲核加成
组合化学
钳子运动
自由基反应
过渡金属卡宾配合物
催化作用
硼
作者
Yubing Pang,Zeyu Ma,Juntao Ye
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2025-10-27
卷期号:58 (02): 195-203
被引量:1
摘要
Abstract Dearomative hydroboration of arenes using nucleophilic boryl radicals provides a powerful strategy for converting flat, abundant arenes into valuable, three-dimensional organoboron architectures. While such reactions are well established for electron-deficient arenes, the analogous transformation of electron-rich heteroarenes remains challenging due to a polarity mismatch. Herein, we report a photocatalytic approach that enables the regioselective, dearomative hydroboration of both electron-rich and electron-deficient indoles and benzofurans using N-heterocyclic carbene boranes. Density functional theory calculations indicate that the C2 addition of the boryl radical is kinetically favored over the C3 addition, and that the addition step becomes irreversible due to a subsequent, low-barrier hydrogen-atom-transfer event.
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