On August 20, 2021, Wang, Tao; Tang, Zongyuan; Luo, Han; Tian, Yi; Xu, Mingchuan; Lu, Qixing; Li, Baosheng published an article.HPLC of Formula: 5301-96-2 The title of the article was Access to (Z)-β-Substituted Enamides from N1-H-1,2,3-Triazoles. And the article contained the following:
A direct ring-opening/nucleophilic substitution reaction of N1-H-1,2,3-triazoles was described. Divergent (Z)-β-halogen- or sulfonyl-substituted enamides were stereospecifically synthesized in a tunable manner. This strategy might not only enable a new ring-opening method of N1-H-1,2,3-triazoles under non-metal catalysis and mild reaction conditions but also offer a good opportunity to reliably access versatile (Z)-β-substituted enamides that could be used as synthetic precursors for further synthetic transformations. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).HPLC of Formula: 5301-96-2
The Article related to acyl halide triazole tandem diastereoselective ring opening nucleophilic substitition, halovinyl amide preparation, sulfonate acyl chloride triazole multicomponent tandem ring opening substitition, amido vinylsulfonate preparation diastereoselective and other aspects.HPLC of Formula: 5301-96-2
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics