95308-77-3

Upstream product

• 1733-63-7 1,2,2-triphenylethan-1-one 
• 62-53-3 aniline 
• 95308-78-4 N-phenylamino-1 triphenyl-1,2,2 ethylene 
• 100-63-0 phenylhydrazine 
• 95268-17-0 (N-methyl N-phenyl)amino-1 triphenyl-1,2,2 ethylene 

Downstream Products

• 201-67-2 13H-13-aza-indeno[1,2-l]phenanthrene 
• 3469-20-3 2,3-diphenyl-1H-indole 

Relevant academic research and scientific papers

The Unusual Anodic Reactivity of Tertiary Enamines in the Presence of Base: the Effect of the Nature of the Base on the Product Distribution

The anodic oxidation of aromatic N-methyl-N-phenylenamines leads to dimers and trimers in the presence of K2CO3, whereas in the presence of 2,6-lutidine demethylation occurs and, in one case, this is subsequent to cyclisation and results in a new 3H-indole.

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.