催化作用
区域选择性
组合化学
化学
过渡金属
卡宾
硼烷
有机合成
氢原子
光化学
纳米技术
有机化学
材料科学
硼
烷基
作者
Wengang Xu,Heming Jiang,Jing Leng,Han Wee Ong,Jie Wu
标识
DOI:10.1002/anie.201911819
摘要
Fluorinated organoboranes serve as versatile synthetic precursors for the preparation of value-added fluorinated organic compounds. Recent progress has been mainly focused on the transition-metal catalyzed defluoroborylation. Herein, we report a photocatalytic defluoroborylation platform through direct B-H activation of N-heterocyclic carbene boranes, through the synergistic merger of a photoredox catalyst and a hydrogen atom transfer catalyst. This atom-economic and operationally simple protocol has enabled defluoroborylation of an extremely broad scope of multifluorinated substrates including polyfluoroarenes, gem-difluoroalkenes, and trifluoromethylalkenes in a highly selective fashion. Intriguingly, the defluoroborylation protocol can be transition-metal free, and the regioselectivity obtained is complementary to the reported transition-metal-catalysis in many cases.
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