环丙烷化
化学
二氯甲烷
激进的
烯烃
催化作用
路易斯酸
有机化学
药物化学
亲核细胞
级联
自由基反应
反应性(心理学)
二碘甲烷
卡宾
光化学
组合化学
保护组
作者
Chang-Zhen Fang,Hong Liu,Zi-Hao Xia,HW Kong,Yan Zhang,Qiang Liu,You-Feng Han,Zhi-Xiang Wang,Xiang-Yu Chen
出处
期刊:Organic Letters
[American Chemical Society]
日期:2026-01-23
卷期号:28 (5): 1893-1898
被引量:3
标识
DOI:10.1021/acs.orglett.6c00039
摘要
Ligated boryl radicals (LBRs), generated from Lewis base-coordinated boranes, have emerged as powerful tools capable of halogen-atom transfer (XAT) processes. Nevertheless, metal-free LBR-enabled radical chemistry remains largely confined to radical additions or cascade pathways. Herein, we report a green-light-induced cyclopropanation of alkenes using dichloromethane (DCM) as a C1 synthon, enabled by the synergistic action of N-heterocyclic nitrenium (NHN) catalysts and LBRs. This work demonstrates a transition-metal-free cyclopropanation of alkenes with DCM, further highlighting the synthetic potential of the NHN/LBR cooperative strategy.
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