In 2019,Organic Letters included an article by Wang, Jing-Hao; Lei, Tao; Nan, Xiao-Lei; Wu, Hao-Lin; Li, Xu-Bing; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu. Recommanded Product: 1H-1,2,3-Triazole. The article was titled 《Regioselective Ortho Amination of an Aromatic C-H Bond by Trifluoroacetic Acid via Electrochemistry》. The information in the text is summarized as follows:
Aryl ethers such as anisole underwent regioselective electrochem. ortho-amination/arylation with pyrazoles and aromatic nitrogen heterocycles mediated by trifluoroacetic acid (TFA) in an undivided cell to give arylpyrazoles such as 1-(2-methoxyphenyl)pyrazole and arylated nitrogen heterocycles. The results came from multiple reactions, including the reaction of 1H-1,2,3-Triazole(cas: 288-36-8Recommanded Product: 1H-1,2,3-Triazole)
1H-1,2,3-Triazole(cas: 288-36-8) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Recommanded Product: 1H-1,2,3-Triazole
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics