I 2 -catalyzed synthesis of 3-aminopyrrole with homopropargylic amines and nitrosoarenes.
Jiaze QinShixuan JiangXiaofeng LuoTianqiang WangPeihua LiuBingxiang YuanRulong YanPublished in: Chemical communications (Cambridge, England) (2024)
The synthesis of 3-aminopyrrole using the amination reagent nitrosoarenes and homopropargylic amines catalyzed by I 2 through cyclization and amination has been developed. This protocol features excellent functional group tolerance and mild reaction conditions, yielding 3-aminopyrroles in moderate to good yields without a metal catalyst. This method realizes the construction and amination of the 3-aminopyrroles in which nitrosoarenes serve as the amine source and oxidant.