108893-53-4

Upstream product

• 91-00-9 Benzhydrylamine 
• 2393-23-9 4-methoxy-benzylamine 
• 123-11-5 4-methoxy-benzaldehyde 
• 805316-34-1 (E)-N-(4-methoxybenzylidene)-1,1-diphenylmethanamine 
• 119-61-9 benzophenone 
• 98-88-4 benzoyl chloride 
• 78999-89-0 N-(diphenylmethylene)-1-(4-methoxyphenyl)methanamine 

Downstream Products

• 22711-21-3 4-methoxybenzil 
• 106349-98-8 5-benzoyl-4-(p-methoxyphenyl)-2,2,5-triphenyl-2,5-dihydro-oxazole 
• 119-61-9 benzophenone 
• 38828-29-4 α-benzoyloxy-4-methoxy-deoxybenzoin 

Relevant academic research and scientific papers

Aroylation of Carbanions Derived from N-(Diphenylmethyl)arylmethanimines. A Synthesis of 4-Aroyloxy-2-azabuta-1,3-dienes

The acylation of carbanions derived from N-(diphenylmethyl)arylmethanimines using aroyl chlorides, allows the preparation of a new type of substituted 2-azabuta-1,3-dienes in which the imino group is conjugated with an enol ester.The reaction is quite general and facilitates the preparation of a wide range of 2-azadienes with electron-donating and electron-withdrawing groups on the phenyl rings.The site selectivity for the attack of the electrophile on the aza-allyl anion can be controlled by the substituents on the carbanion and on the hardness of the electrophile.

Aroylation of n-alkylmethanimines. A synthesis of novel substituted 2-aza-buta-1,3-dienes.

The aroylation of carbanions derived from N-benzyl-diphenylmethanimine and N-(diphenylmethyl )-arylmethanimines yields highly substituted 2-aza-buta- 1,3-dienes in which the imino group is conjugated with an enol ester. A similar reaction with N-(diphenyl