17260-48-9

Upstream product

• 941-55-9 4-toluenesulfonyl azide 
• 7196-01-2 4-(1-phenylvinyl)morpholine 
• 70-55-3 toluene-4-sulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 127-65-1 chloroamine-T 
• 100-52-7 benzaldehyde 
• 2032-36-2 Thiobenzmorpholid 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 4176-68-5 (Z)-1-(1,2-diphenylvinyl)morpholine 
• 64274-09-5 4-(1-phenyl-but-1-enyl)-morpholine 

Downstream Products

• 10316-00-4 4-benzyl-morpholine 

Relevant academic research and scientific papers

Zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides: A new approach to the synthesis of amidines

The first zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides is described. Various thioamides were reacted with N-arylsulfonyl aziridines in the presence of a catalytic amount of dry zinc chloride to provide the corresponding

Facile synthesis of sulfonyl amidines and β-amino sulfonyl enamines under transition-metal-free conditions

Treatment of enamine and azide resulted in the formation of either sulfonyl amidine or β-amino sulfonyl enamine derivative in moderate to good yields. The reaction could proceed under catalyst-free conditions. Georg Thieme Verlag Stuttgart · New York.