化学
激进的
光催化
光化学
氧化磷酸化
组合化学
有机化学
产量(工程)
分子
催化作用
作者
Yu Matsuda,Takahito Kuribara,Tetsuhiro Nemoto
出处
期刊:Organic Letters
[American Chemical Society]
日期:2026-04-24
卷期号:28 (18): 5865-5869
标识
DOI:10.1021/acs.orglett.6c01460
摘要
Phosphine-boryl radicals remain less well-studied because their parent phosphine-boranes are highly stable under oxidative conditions. Herein, we report a strategy for generating phosphine-boryl radicals facilitated by radical precursors through an appropriate molecular design. Incorporating a proximal oxidant into a phosphine-borane facilitates the formation of the corresponding boron-centered radical through proton-coupled intramolecular electron transfer. The resulting phosphine-boryl radical can be used to generate an alkyl radical via halogen atom transfer.
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