128229-15-2Relevant academic research and scientific papers
Triazolines XVIII. Nickel peroxide oxidation of 4,5-dihydro-1H-1,2,3-triazoles bearing sterically crowded ortho-substituted 5-phenyl groups
Kadaba,Edelstein
, p. 191 - 192 (1990)
Nickel peroxide functions as an efficient oxidizing agent, superior to permanganate (phase-transfer catalytic system), in the oxidative dehydrogenation of 4,5-dihydro-1H-1,2,3-triazoles 1a-1, bearing sterically crowded ortho-substituted 5-phenyl groups, t
Triazolines. 19. Nickel Peroxide Oxidation of Δ2-1,2,3-Triazolines. A Versatile General Synthetic Route to 1H-1,2,3-Triazoles
Kadaba, Pankaja K.,Edelstein, Steven B.
, p. 5891 - 5894 (2007/10/02)
Although the oxidative dehydrogenation of Δ2-1,2,3-triazolines using potassium permanganate in a phase-transfer catalyzed reaction system affords a convenient route for the synthesis of a number of 1-aryl-5-heteroaryl-substituted 1H-1,2,3-triaz
