77014-38-1

Upstream product

• 16979-20-7 N-(4-methylbenzylidene)-4-methylaniline 

Downstream Products

• 77014-42-7 1,3,4,5-Tetra-p-tolyl-1,3-dihydro-imidazol-2-one 
• 1051966-36-9 1,3,4,5-tetra(4-methylphenyl)-1H-imidazolium chloride 
• 97531-34-5 2-Ethoxy-2-oxo-1,3,4,5-tetrakis<4-methylphenyl>-2,3-dihydro-1H-P^V-1,3,2-diazaphosphole 

Relevant academic research and scientific papers

Synthesis of electronically diverse tetraarylimidazolylidene carbenes via catalytic aldimine coupling

(Chemical Equation Presented) A new method for synthesizing symmetrical N-heterocyclic imidazolium salts is described. Catalytic coupling of aldimines with cyanide followed by oxidation gives α-diketimines, which can then be cyclized with formaldehyde in

A novel reductive dimerization/oxidative dehydrogenation of aldimines mediated by lanthanoid metals

A lanthanoid metal-mediated novel reductive dimerization/oxidative dehydrogenation of a variety of aldimines has been achieved. Aromatic aldimines (1) were dimerized in the presence of 0.5 mol of ytterbium metal (Yb) and 1-naphthaldehyde (1-NpCHO) to give

NOVEL AND CONVENIENT SYNTHESES OF SUBSTITUTED 1,4-DIAZOCINES AND 1,4-DIAZONINES

Treatment of dianils with sodium in dry ether followed by addition of 1,4-dichlorobutane and 1,5-dichloropentane gave 1,2,3,4-tetraaryl-1,4,5,6,7,8-hexahydro-1,4-diazocines and 1,2,3,4-tetraaryl-4,5,6,7,8,9-hexahydro-1H-1,4-diazonines respectively.