Affiliation:
1. State Key Laboratory and Institute of Elemento-Organic Chemistry College of Chemistry Nankai University Tianjin 300071 China
2. Frontiers Science Center for New Organic Matter Nankai University Tianjin 300071 China
3. Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192 China
Abstract
AbstractHerein, 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.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献