摘要
A novel and metal-free synthetic method for the formation of pyrrolo[1,2-a]imidazol-7-one or pyrrol-3-one from dihydropyrroloimidazol-6-one through the C-N bond cleavage and formation was achieved. The salient features of this method are operational simplicity, mild reaction conditions, and readily available starting materials.
- 出版日期2016-9-7
- 单位华东理工大学