On December 31, 2017, Gui, Yong-Yuan; Chen, Xiao-Wang; Zhou, Wen-Jun; Yu, Da-Gang published an article.Recommanded Product: N,N-Diethylacetamide The title of the article was Arylation of Amide and Urea C(sp3)-H Bonds with Aryl Tosylates Generated In Situ from Phenols. And the article contained the following:
The arylation of amide and urea C(sp3)-H bonds with aryl tosylates generated in situ from phenols has been realized at room temperature by combining visible-light-photoredox catalysis, hydrogen-atom-transfer catalysis, and nickel catalysis. This streamlined protocol permits rapid functionalization of phenols and direct transformation of 伪-amino C(sp3)-H bonds. The C(sp3)-H arylation products are obtained in high yields with good functional-group tolerance at low catalyst loadings. The experimental process involved the reaction of N,N-Diethylacetamide(cas: 685-91-6).Recommanded Product: N,N-Diethylacetamide
The Article related to amide urea arylation aryl tosylate, photoredox hydrogen atom transfer nickel catalysis, General Organic Chemistry: Synthetic Methods and other aspects.Recommanded Product: N,N-Diethylacetamide
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics