206360-93-2

Upstream product

• 1746-13-0 allyl phenyl ether 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 119350-41-3 N-(2-hydroxy-3-phenoxypropyl)-4-methylbenzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 122-60-1 Phenyl glycidyl ether 
• 1026605-15-1 1-N-(4-methylphenylsulfonyl)amino-2-O-(4-methylphenylsulfonyl)oxy-3-(phenoxy)propane 

Downstream Products

• 206361-11-7 N-Allyl-4-methyl-N-(1-phenoxymethyl-2-phenylselanyl-ethyl)-benzenesulfonamide 
• 206361-03-7 4-Methyl-N-(1-phenoxymethyl-2-phenylselanyl-ethyl)-benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis of N-sulfonyl aziridines through regioselective opening of epoxides under solid-liquid PTC conditions

The ring opening of epoxides 1 with 4-toluenesulfonamide (6) under solid-liquid phase transfer catalysis (SL-PTC) conditions afforded regioselectively β-sulfonamidoalcohols 7 in high yields. These were further convened into N-sulfonylaziridines 9 after ac

Pyrrolidines from olefins via radical cyclization

2,4-Disubstituted N-tosylpyrrolidines were prepared from olifeins via N- tosylaziridination, benseneselenolate ring-opening and reductive radical cyclization. Azidoselenation of olefins, followed by reduction, N-tosylation, N-allylation and reductive radical cyclization, afforded 3,4-disubstituted N- tosylpyrrolidines.