4.7 Article

Nickel-Catalyzed Amination of Aryl Nitriles for Accessing Diarylamines through C-CN Bond Activation

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 363, Issue 20, Pages 4708-4713

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202100641

Keywords

Amination; C-CN bond activation; Nickel; Diarylamines; Aryl nitriles

Funding

  1. National Natural Science Foundation of China [21773210, 21972125, 21776260]
  2. Fundamental Research Funds for the Provincial University of Zhejiang [RF-B2019005]

Ask authors/readers for more resources

A new nickel-catalyzed amination method has been developed for the synthesis of diarylamines through C-CN bond activation of aryl nitriles with anilines. Various aromatic and heteroaromatic nitriles were used as electrophiles to couple with substituted anilines, resulting in a diverse range of diarylamines with yields ranging from 15% to 95%.
A nickel-catalyzed amination to access diarylamines has been developed through C-CN bond activation of aryl nitriles with anilines. In this developed catalytic protocol, various aromatic and heteroaromatic nitriles could be utilized as the electrophiles to couple with substituted anilines. A diversity of diarylamines were obtained in 15-95% yields.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available