121838-18-4

Upstream product

• 1605-08-9 cis-2-benzyl-3-phenylaziridine 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 121846-96-6 N-((1R,2R)-1-Benzyl-2-ethoxy-2-phenyl-ethyl)-benzenesulfonamide 
• 121846-97-7 threo-N-(1,3-diphenyl-2-methoxypropyl)benzenesulfonamide 
• 121846-95-5 threo-N,N'-(1-benzyl-2-phenyl-1,2-ethanediyl)bis(benzenesulfonamide) 
• 121846-94-4 N-[(2E)-1,3-diphenyl-2-propen-1-yl]benzenesulfonamide 
• 121846-93-3 cis-N-(1,3-diphenylallyl)benzenesulfonamide 
• 1083-30-3 dihydrochalcone 
• 1605-08-9 cis-2-benzyl-3-phenylaziridine 
• 121846-92-2 threo-N-(1,3-diphenyl-2-methoxypropyl)benzenesulfonamide 
• 121838-20-8 N-((1R,2R)-1-Benzyl-2-methoxy-2-phenyl-ethyl)-benzenesulfonamide 
• 84-65-1 9,10-phenanthrenequinone 
• 136175-24-1 erythro-9-<1,3-diphenyl-2-(phenylsulfonamido)propyl>-9,10-dihydroanthracene 

Relevant academic research and scientific papers

Reactions with Aziridines, XLVII: Regiospecificity and Stereoselectivity of Acid Catalyzed Alcoholysis of cis-2-Benzyl-3-phenyl-1-phenylsulfonylaziridine

In ROH/H2SO4 the title compound is exclusively cleaved between N and C-3 yielding predominantly one diastereomer so that only a small portion of ring opening can proceed via a free carbenium ion.Ring opening shows an inverse dependence on the size of R.