92939-24-7

Upstream product

• 667-14-1 N-benzoyl-p-toluene sulfonimidoyl chloride 
• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 52730-78-6 (+)-(S)-N-[carbo-(1R)-menthoxy]-p-toluenesulfonimidoyl chloride 
• 52720-06-6 C₉H₁₄N₂OS 
• 1050610-05-3 C₁₆H₁₈N₂O₂S 

Downstream Products

• 104415-73-8 C₉H₁₃ClN₂OS 

Relevant academic research and scientific papers

A convenient synthetic route to sulfonimidamides from sulfonamides

Sulfonimidamides were prepared in a one-pot transformation from sulfonamides, through nucleophilic substitution of sulfonimidoyl chlorides formed in situ with different amines. This methodology represents a convenient, safe, and easily accessible synthetic route to sulfonimidamides.

DERIVATIVES OF SULFONIMIDIC ACIDS. N1,N1-DIALKYL-N2-CHLOROARENESULFONIMIDAMIDES

N1,N1-Dialkyl-N2-chloroarenesulfonimidamides were obtained by the reaction of N1,N1-dialkylarenesulfonimidamides with tert-butyl hypochlorite or N,N-dichlorobenzenesulfonamide.With triphenylphosphine or dimethyl sulfide they form onium salts.In dimethylsulfonium chlorides, which contain a chiral sulfur atom, the methyl groups of the dimethylsulfonium group are diastereotopic.