147383-20-8

Upstream product

• 1025877-31-9 C₁₇H₂₁NO₆S₃ 
• 42153-74-2 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfoximide 
• 127-65-1 chloroamine-T 
• 10330-22-0 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfilimine 
• 100-68-5 methyl-phenyl-thioether 
• 75-07-0 acetaldehyde 

Downstream Products

• 181268-60-0 S-Phenyl-S-(1-trimethylsilyl-2-methyl)hexyl-N-(toluene-p-sulfonyl)sulfoximine 
• 181268-58-6 S-Phenyl-S-(1-trimethylsilyl-2-phenyl)propyl-N-(toluene-p-sulfonyl)sulfoximine 
• 181268-46-2 S-Phenyl-S-((E)-1-trimethylsilylprop-1-enyl)-N-(toluene-p-sulfonyl)sulfoximine 
• 127680-68-6 S-(trans-3-methyl-2-oxiranyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximide 

Relevant academic research and scientific papers

An efficient preparation of β-dimethylaminovinyl sulfone and sulfoximide, and investigation of their reactivity as dipolarophiles

A simple reaction affording (E)-1-dimethylamino-2-phenylsulfonylethylene, and S-((E)-2-(N′N′-dimethylamino)ethenyl)-5-phenyl-N-(p- tolylsulfonyl) sulfoximide in high yields is described. A reversal in regioselectivity was observed when the ss-dimethylamin

Synthesis and Highly Diastereoselective Nucleophilic Epoxidation of N-(p-Tolylsulfonyl)vinylsulfoximines

N-(p-Tolylsulfonyl)vinylsulfoximines 3 may be prepared in good yield in a one-pot process by reaction of lithiated S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfoximine with aldehydes, followed by elimination using methanesulfonyl chloride-triethylamine.The vi

Very High Diastereofacial Selectivity in the Nucleophilic Epoxidation of N-(p-Tolylsulphonyl)vinylsulphoximines

Nucleophilic epoxidation of N-(p-tolylsulphonyl)vinylsulphoximines (6) using lithium t-butylhydroperoxide proceeds with very high diastereofacial selectivity, the sense of which was established by a single crystal X-ray structure determination, to give N-