1186338-75-9Relevant academic research and scientific papers
Ambient benzotriazole ring opening through intermolecular radical addition to vinyltriazole
Su, Yijin,Petersen, Jeffrey L.,Gregg, Tesia L.,Shi, Xiaodong
, p. 1208 - 1211 (2015)
Radical addition to vinyltriazole was developed as a new approach to achieve 1,2,3-triazole ring opening under mild conditions. Through reagent control, excellent chemoselectivity was achieved, giving either nitrile under basic conditions or quinoxaline under neutral conditions. Reactivities made this method an attractive new reaction mode.
An organoselenium-catalyzed N1- And N2-selective aza-Wacker reaction of alkenes with benzotriazoles
Sun, Kai,Wang, Qinlin,Wang, Xin,Wu, Lanlan,Xue, Yanru,Zhang, Bing
supporting information, p. 4436 - 4439 (2020/05/05)
An organoselenium-catalyzed N1- and N2-selective aza-Wacker reaction of alkenes with benzotriazoles is reported, which provides easy access to N1- and N2-olefinated benzotriazole derivatives. The wide substrate
Highly efficient synthesis of vinyl substituted triazoles by Au(I) catalyzed alkyne activation
Duan, Haifeng,Yan, Wuming,Sengupta, Sujata,Shi, Xiaodong
supporting information; experimental part, p. 3899 - 3902 (2010/03/25)
Au(I) catalyzed 1,2,3-triazole addition to non-activated alkyne was reported. A large group of substituted NH-1,2,3-triazoles were suitable for this transformation along with both internal and terminal alkynes. The N-1 and N-2 vinyl substituted 1,2,3-tria
