吲哚
分子内力
戒指(化学)
化学
序列(生物学)
立体化学
组合化学
有机化学
生物化学
作者
Hai‐Shan Jin,Qing‐Yun Fang,Jin‐Qi Wang,Li‐Ming Zhao
标识
DOI:10.1002/chem.202300467
摘要
A divergent reaction of indoline-derived azadienes with α-bromohydroxamates for the selective synthesis of spiro-indolinepyrrolidinones and indoline-fused diazepinones was disclosed. This reaction sequence involved an initial formation of five-membered spirocyclic products followed by an intramolecular ring-opening and ring expansion to produce seven-membered diazepinones. We demonstrated that controlling the reaction time could modulate the reaction pathway for formation of different molecular frameworks for the same set of substrates. Based on the experimental results, the reaction mechanism was also discussed and proposed to explain the phenomena observed in the process.
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