69085-78-5

Upstream product

• 78523-84-9 2,4,5-triphenyl-3-phenyliminoisoxazoline 
• 78523-82-7 N-phenyl-N-(1-phenylimino-2-benzoyl-2-phenylethyl)hydroxylamine 
• 622-16-2 1,3-Diphenylcarbodiimide 
• 1484-50-0 desyl bromide 
• 69085-77-4 2-benzoyl-N,2-diphenylvinylideneamine 
• 100-65-2 N-Phenylhydroxylamine 
• 4198-95-2 α-phenylimino-deoxybenzoin 
• 622-44-6 phenylcarbonimidic dichloride 

Downstream Products

• 74720-14-2 N-(α-benzoylbenzyl)-NN'-diphenylurea 
• 74720-15-3 5-hydroxy-1,3,4,5-tetraphenylimidazolidin-2-one 
• 74720-16-4 N-(1-phenylstyryl)-NN'-diphenylurea 
• 74720-17-5 N-(1,2-diphenylethyl)-NN'-diphenylurea 
• 14279-02-8 2-oxo-1,3,4,5-tetraphenyl-2,3-dihydroimidazole 
• 102-07-8 bis(diphenyl)urea 

Relevant academic research and scientific papers

Electrochemical Synthesis and X-Ray Molecular Structure of 3,4,5-Triaryl-2-Aryliminooxazolines

Selective cathodic reduction of benzilmonoimines in aprotic medium at a mercury pool cathode, under constant potential, in the presence of equimolecular amounts of N-arylcarbonimidoyl dichlorides, provides a new and very convenient method for the synthesi

Keteimines as Intermediates to Heterocycles. Part 3. Rearrangement of 3-Iminoisoxazolines to 2-Imino-oxazolines

N-Substituted hydroxylamines (2) add to 2-benzoyl-N,2-diphenylvinylideneamine (1) and the adducts are easily dehydrated to give the 3-iminoisoxazolines (4).Compounds (4) with 2-aryl substituents rearrange spontaneously to give the 2-imino-oxazolines (5) or (6), but the 2-methyl derivative is more stable and only rearranges on heating. 2-Imino-3-acylaziridines (8) or (9) are assumed to be the intermediates; the expected 2-imino-oxazoline (5b) was isolated among the products during an attempted synthesis of 1,3-diphenyl-2-phenylimino-3-benzoylaziridine (8b) from benzoylphenylcarbene and diphenylcarbodi-imide.