化学
烷基化
基础(拓扑)
氢原子
Atom(片上系统)
药物化学
立体化学
催化作用
有机化学
群(周期表)
数学
计算机科学
数学分析
嵌入式系统
作者
Meifang Tang,Bingbing Feng,Yanyang Bao,Zhongtian Xu,Chao Huang,Hanliang Zheng,Gangguo Zhu,Yanan Wang,Zheliang Yuan
标识
DOI:10.1002/cjoc.202400122
摘要
Comprehensive Summary Compared to well‐established 1,5‐HAT of N ‐centered radicals, the synthetic applications of 1,2‐HAT process were scarce due to the high barrier and constrained three‐membered transition state. Here, we have developed a novel C(sp 3 )‐H gem ‐difluoroallylation via a base assisted formal 1,2‐HAT of amidyl radicals with the reductive quenching cycle of photocatalyst. This transformation enables the efficient formation of α‐aminoalkyl radicals via 1,2‐HAT and showcases good functional group tolerance. Our preliminary mechanistic experiments, along with Density Functional Theory (DFT) calculations demonstrate the feasibility of 1,2‐HAT of amidyl radicals, especially when assisted by a base. Furthermore, our method also succeeds in the Giese addition of electron‐deficient alkenes as well as styrene.
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