Abstract
Herein, we report that bulky alkylphosphines such as PtBu3 can switch the roles from actor to spectator ligands to promote the FeCl2-catalyzed N-amidation reaction of arylamines with dioxazolones, giving hydrazides in high efficiency and chemoselectivity. Mechanistic studies indicated that the phosphine ligands could facilitate the decarboxylation of dioxazolones on the Fe center, and the hydrogen bonding interactions between the arylamines and the ligands on Fe nitrenoid intermediates might play a role in modulating the delicate interplay between the phosphine ligand, arylamine, and acyl nitrene N, favoring N−N coupling over N−P coupling. The new ligand-promoted N-amidation protocols offer a convenient way to access various challenging triazane compounds via double or sequential N-amidation of primary arylamines.
Author supplied keywords
Cite
CITATION STYLE
Zhu, S. Y., He, W. J., Shen, G. C., Bai, Z. Q., Song, F. F., He, G., … Chen, G. (2024). Ligand-Promoted Iron-Catalyzed Nitrene Transfer for the Synthesis of Hydrazines and Triazanes through N-Amidation of Arylamines. Angewandte Chemie - International Edition, 63(2). https://doi.org/10.1002/anie.202312465
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.