School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, 221116, Jiangsu, P. R. China.
State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, P. R. China.
Chemistry. 2023 Jun 2;29(31):e202300467. doi: 10.1002/chem.202300467. Epub 2023 Apr 20.
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.
一种吲哚衍生的氮杂二烯与α-溴代羟胺酸的发散反应,用于选择性合成螺吲哚吡咯烷酮和吲哚并二氮杂酮。该反应序列涉及五元螺环产物的初始形成,然后进行分子内环开环和环扩张,生成七元二氮杂酮。我们证明,控制反应时间可以调节反应途径,从而在同一组底物上形成不同的分子骨架。基于实验结果,还讨论了反应机理,并提出了该过程中观察到的现象的解释。