67087-35-8

Upstream product

• 100-68-5 methyl-phenyl-thioether 

Downstream Products

• 72277-50-0 C₁₃H₂₀ClNOS 
• 54090-90-3 N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)benzamide 
• 1377585-41-5 3-methyl-N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)benzamide 
• 1426922-71-5 N-(3-chlorobenzoyl)-S-methyl-S-phenyl sulfoximine 
• 1572535-22-8 3-bromo-N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)benzamide 
• 1377585-47-1 4-methyl-N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)benzamide 
• 1377585-49-3 4-chloro-N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)benzamide 
• 1572535-33-1 4-bromo-N-(methyl(oxo)(phenyl)-λ6-sulfanylidene)benzamide 
• 1572535-35-3 N-(4-iodobenzoyl)-S-methyl-S-phenyl sulfoximine 
• 50597-21-2 N-(methyl(oxo)(phenyl)-λ⁶-sulfanylidene)-4-nitrobenzamide 
• 1572535-42-2 C₁₅H₁₅NO₅S₂ 
• 1572535-46-6 N-(3-bromo-5-methylbenzoyl)-S-methyl-S-phenylsulfoximine 
• 1572535-49-9 N-(3-iodo-5-methylbenzoyl)-S-methyl-S-phenylsulfoximine 
• 1572535-53-5 3,5-dimethyl-N-(methyl(oxo)(phenyl)-λ6-sulfanylidene)benzamide 

Relevant academic research and scientific papers

One-Pot Synthesis of N-Iodo Sulfoximines from Sulfides

This is the first report on the synthesis and characterization of N-iodo sulfoximines. The synthesis was designed as a room temperature one-pot cascade reaction from readily available sulfides as starting compounds, converted into sulfoximines by reaction with ammonium carbonate and (diacetoxyiodo)benzene, followed by iodination with N-iodosuccinimide or iodine in situ, in up to 90% isolated yields, also at a multigram scale. Iodination of aryls with N-iodo sulfoximines, oxidation, and conversion to N-SCF3 congeners have been demonstrated.