Iodine pentoxide-mediated oxidative selenation and seleno/thiocyanation of electron-rich arenes.
Yong-Hao WangYun-Qian ZhangChen-Fan ZhouYou-Qin JiangYue XuXiaobao ZengGong-Qing LiuPublished in: Organic & biomolecular chemistry (2022)
A simple and efficient method for the regioselective selenation of electron-rich arenes by employing non-metal inorganic iodine pentoxide (I 2 O 5 ) as a reaction promoter under ambient conditions has been developed. The present protocol showed broad functional group tolerance and easy-to-operate and time-economical features. Additionally, this protocol also allows access to 3-seleno and 3-thiocyanoindoles by the use of readily available selenocyanate and thiocyanate salts. A mechanistic study indicated that the transformation operated through selenenyl iodide-induced electrophilic substitution processes.