<i>In Situ</i> Generation of <i>N</i>-Triflylimino-λ<sup>3</sup>-iodanes: Application to Imidation of Phosphines and Catalytic α-Amidation of 1,3-Dicarbonyl Compounds

Shun Sunagawa, Fumiya Morisaki, Takafumi Baba, Akira Tsubouchi, Akira Yoshimura, Kazunori Miyamoto, Masanobu Uchiyama, Akio Saito

Organic Letters · 2022 · 12 citations · 51 references

Abstract

We describe the imidation of phosphines and α-amidation of 1,3-dicarbonyl compounds using <i>N</i>-triflylimino-λ<sup>3</sup>-iodane, which is generated <i>in situ</i> from iodosylarene and triflylamide without any other additives. Furthermore, the imino-λ<sup>3</sup>-iodane catalytically generated from an iodoarene precatalyst with oxone and triflylamide promotes α-amidation of 1,3-dicarbonyl compounds, representing the first method catalyzed by imino-λ<sup>3</sup>-iodane.

References

51