In 2019,Organic Letters included an article by Roshandel, Sahar; Lunn, Maiko J.; Rasul, Golam; Muthiah Ravinson, Daniel Sylvinson; Suri, Suresh C.; Prakash, G. K. Surya. SDS of cas: 288-36-8. The article was titled 《Catalyst-Free Regioselective N2 Arylation of 1,2,3-Triazoles Using Diaryl Iodonium Salts》. The information in the text is summarized as follows:
The widespread application of 1,2,3-triazoles in pharmaceuticals has resulted in substantial interest toward developing efficient postmodification methods. Whereas there are many postmodification methods available to obtain N1-substituted 1,2,3-triazoles, developing a selective and convenient protocol to synthesize N2-aryl-1,2,3-triazoles has been challenging. A catalyst-free and regioselective method to access N2-aryl-1,2,3-triazoles in good to excellent yields (66-97%), is reported. This scalable postmodification protocol is effective for a wide range of substrates. The experimental process involved the reaction of 1H-1,2,3-Triazole(cas: 288-36-8SDS of cas: 288-36-8)
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 SDS of cas: 288-36-8
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics