环丙烯
烷基
化学
催化作用
选择性
组合化学
卤化物
基质(水族馆)
有机化学
生物
生态学
作者
Zhilin Zhang,Zhen Li,Yuantai Xu,Lu Yu,Jian Kuang,Yan Li,Jia‐Wang Wang,Changlin Tian,Xi Hong Lu,Yao Fu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-05-31
卷期号:62 (30): e202306381-e202306381
被引量:45
标识
DOI:10.1002/anie.202306381
摘要
Cyclopropene hydrofunctionalization has been a promising strategy for accessing multi-substituted cyclopropanes; however, cyclopropene hydroalkylation remains underdeveloped. Herein, we report a low-valent CoH-catalyzed facial-selective cyclopropene hydroalkylation to access multi-substituted cyclopropanes. This reaction exhibits a broad substrate scope of alkyl halides and cyclopropenes and tolerates many functional groups. Moderate-to-good facial-selectivity is obtained without any directing groups. Mechanism studies provide evidence that alkyl radicals are generated from alkyl halides and irreversible CoH insertion is responsible for the facial-selectivity. Our preliminary exploration demonstrates that asymmetric cyclopropene hydroalkylation can be realized without conspicuous auxiliary groups.
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