52806-52-7

Upstream product

• 34918-74-6 N-(4-methoxyphenyl)benzimidoyl chloride 
• 62-53-3 aniline 
• 67-56-1 methanol 
• 53170-30-2 N-Hydroxy-N,N'-diphenylbenzamidin 
• 104-94-9 4-methoxy-aniline 
• 38430-03-4 N-phenylbenzimidoyl chloride 
• 93-98-1 N-phenyl benzoyl amide 
• 98-88-4 benzoyl chloride 
• 413576-78-0 C₂₀H₁₈N₂O*ClH 
• 7472-54-0 C₁₄H₁₃NO₂ 
• 7472-54-0 N-(p-methoxyphenyl)benzamide 

Relevant academic research and scientific papers

Highly active nano-MgO catalyzed, mild, and efficient synthesis of amidines via electrophilic activation of amides

Nano-MgO catalyzed synthesis of amidine derivatives is developed under solvent-free reaction condition at 70 C. Reusability of the catalyst and shorter reaction time as well as high yields are the advantages of this procedure.

Synthesis, antileishmanial activity and structure-activity relationship of 1-N-X-phenyl-3-N′-Y-phenyl-benzamidines

Two series of N,N′-diphenyl-benzamidines were synthesized as part of a study to search potential new drugs with antileishmanial activity. These compounds were obtained by anilides in PCl5 halogenation reaction with generation in situ of the cor

Memory Effects and 1,3-Diazepine Ring Closure in Arylnitrenium Ions

15N- and 18O-Labelling experiments demonstrate that in the aromatic rearrangement of N,N'-diphenyl-N-(4-tosyloxy)benzamidines (2 -> 3 - 6) a strong memory effect occurs in oriented contact ion pairs.The formation of 1,3-diazepines 9 by ring closure betwee