Iron-Catalyzed Intramolecular C-H Amination of α-Azidyl Amides.

@article{Zhao2019IronCatalyzedIC,
  title={Iron-Catalyzed Intramolecular C-H Amination of α-Azidyl Amides.},
  author={Xiaopeng Zhao and Siyu Liang and Xing Fan and Tonghao Yang and Wei Yu},
  journal={Organic letters},
  year={2019},
  volume={21 6},
  pages={
          1559-1563
        }
}
Iron-catalyzed intramolecular C-H amination of aliphatic azides has recently emerged as a powerful tool for the preparation of nitrogen heterocycles. This paper reports that α-azidyl amides can be converted in high efficacy to imidazolinone compounds via intramolecular C(sp3)-H amination by the action of a simple catalytic system composed of FeCl2 and a β-diketiminate ligand. The reactions provide a simple and atom-economical approach toward polysubstituted imidazolinones. 
12 Citations
Iron-catalysed 1,2-aryl migration of tertiary azides.
Tricyclic Imidazolidin-4-ones by Witkop Oxidation of Tetrahydro-β-carbolines.
...
1
2
...