1378302-79-4

Upstream product

• 1438414-24-4 N-(4-methoxyphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 62-53-3 aniline 
• 100-68-5 methyl-phenyl-thioether 

Downstream Products

• 1378303-45-7 (R)-N-H-N'-phenyl-S-methyl-S-phenylsulfodiimide 
• 1378303-44-6 (S)-N-H-N'-phenyl-S-methyl-S-phenylsulfodiimide 
• 1378303-35-5 N-phenyl-N'-cyano-S-methyl-S-phenyl sulfondiimine 
• 1378303-42-4 N-phenyl-N'-(2-nitrophenyl)-S-methyl-S-phenyl sulfondiimine 
• 1378303-36-6 N-phenyl-N'-acetyl-S-methyl-S-phenyl sulfondiimine 
• 1378303-38-8 N-phenyl-N'-tert-butyldimethylsilyl-S-methyl-S-phenyl sulfondiimine 
• 1378303-40-2 N-propargyl-N’-phenyl-S-methyl-S-phenylsulfondiimine 
• 1438414-39-1 C₂₀H₁₆N₂S 
• 1438414-38-0 N-(2-carbaldehydephenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 1438414-24-4 N-(4-methoxyphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 1438414-25-5 N-(3-methoxyphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 1438414-26-6 N-(2-methoxyphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 1438414-27-7 N-(3-methylphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 
• 1438414-28-8 N-(4-biphenyl)-N'-phenyl-S-methyl-S-phenyl sulfondiimine 

Relevant academic research and scientific papers

Synthesis of sulfondiimines by N-chlorosuccinimide-mediated oxidative imination of sulfiliminium salts

Access to sulfondiimines: The oxidative one-pot chlorination-imination sequence of in situ generated free sulfilimines by N-chlorosuccinimide (NCS) allows the preparation of N-monosubstituted sulfondiimines under mild reaction conditions with excellent functional-group tolerance (see scheme; Mes=2,4,6-trimethylphenylsulfonyl) Copyright

Palladium-catalyzed C-N cross-coupling of N'-monosubstituted sulfondiimines with aryl bromides

A general method for the N-arylation of sulfondiimines with aryl bromides using tris(dibenzylideneacetone)dipalladium(0) [Pd2(dba)3] and 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (RuPhos) as catalyst system was developed. A new benzothiazine was obtained, and a protocol for the cleavage of para-methoxyphenyl (PMP) groups in PMP-protected sulfondiimines has been found, which provides access to synthetically useful NH-derivatives, that are difficult to prepare by other means. Copyright