54212-63-4

Upstream product

• 4706-43-8 1-benzyl-1H-benzotriazole 
• 74-88-4 methyl iodide 
• 71-43-2 benzene 
• 24099-48-7 (Z)-1,2,N,N'-Tetraphenyl-ethene-1,2-diamine 
• 74-87-3 methylene chloride 
• 7510-33-0 N,N'-diphenyl-1,2-diphenylethane-1,2-diimine 
• 54212-62-3 trans-α,β-Bis-(N-methylanilino)-stilben 

Relevant academic research and scientific papers

Mannich/Friedel-Crafts Preparations of 1-(Arylmethyl)benzotriazoles and Synthetic Transformations of their Lithio Derivatives

The synthesis of 1-(arylmethyl)benzotriazoles by Mannich type reactions of benzene, toluene, p-xylene and chlorobenzene with 1-chloromethylbenzotriazole in the presence of aluminium halides is reported.Alkylation of their lithio derivatives followed by th

Enamines et enediamines: synthese et oxydation anodique. Application a la formation de nouveaux heterocycles

The anodic oxidation of certain tertiary enamines and enediamines is particularly sensitive to the medium effect: specific action of bases leading to either dimers or trimers, or to the formation of a new 3 H-indole (case of enamines); reaction with moisture in the solvent allowing the obtention of indolooxazolidines (case of enediamines).The reactivity of the oxidized forms of the substrates is discussed as a function of the nature of the electrolysis medium and the structure of the products amenable to electrolysis.