727-38-8

Upstream product

• 98-10-2 benzenesulfonamide 
• 529-20-4 2-methylphenyl aldehyde 

Downstream Products

• 35921-71-2 N-phenylsulfonyl-o-methylphenyl(phenyl)methylamine 
• 1129549-67-2 C₂₂H₂₁NO₃S₂ 
• 1184294-20-9 3-((4R,5S)-5-(2-methylphenyl)-1-(phenylsulfonyl)-2-thioxoimidazolidine-4-carbonyl)oxazolidin-2-one 
• 1236009-87-2 N-(p-toluenesulfonyl)-2-(2-furanyl)methylaziridine 
• 1236212-79-5 C₂₄H₂₂F₃NO₃S₂ 
• 1236212-78-4 C₂₄H₂₅NO₃S₂ 
• 1437539-84-8 C₂₃H₂₃NO₃S 

Relevant academic research and scientific papers

Visible-light, iodine-promoted formation of n-sulfonyl imines and n-alkylsulfonamides from aldehydes and hypervalent iodine reagents

Alternative synthetic methodology for the direct installation of sulfonamide functionality is a highly desirable goal within the domain of drug discovery and development. The formation of synthetically valuable N-sulfonyl imines from a range of aldehydes,

Nitroxyl-Radical-Catalyzed Oxidative Coupling of Amides with Silylated Nucleophiles through N-Halogenation

A nitroxyl-radical-catalyzed oxidative coupling reaction between amines with an N-protecting electron-withdrawing group (EWG) and silylated nucleophiles was developed to furnish coupling products in high yields, thus opening up new frontiers in organocatalyzed reactions. This reaction proceeded through the activation of N-halogenated amides by a nitroxyl-radical catalyst, followed by carbon–carbon coupling with silylated nucleophiles. Studies of the reaction mechanism indicated that the nitroxyl radical activates N-halogenated amides, which are generated from N-EWG-protected amides and a halogenation reagent, to give the corresponding imines.