化学
分子内力
呋喃
环加成
吲哚试验
组合化学
反应条件
分子内反应
立体化学
对偶(语法数字)
计算化学
双重角色
有机化学
反应中间体
分子
光化学
作者
Jiang Cheng,Wen-Jie Shen,Yuan‐Zheng Cheng,Shu‐Li You
标识
DOI:10.1021/acs.orglett.6c03621
摘要
Abstract Despite significant advances in the field of dearomatization, dual dearomatization remains underdeveloped. Herein, we report an intramolecular dual dearomatization reaction of indoles and furans by photoredox catalysis. This method enables the construction of four fused rings in a single step with exceptional regio- and diastereoselectivities under mild conditions. The products can be converted into furan-fused polycyclic scaffolds in a one-pot procedure by using p-toluenesulfonic acid. The synthetic utility of this approach was demonstrated through gram-scale synthesis and several downstream transformations. Mechanistic studies revealed that this reaction proceeds via a single-electron transfer (SET) pathway rather than an energy transfer pathway.
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