42872-16-2

Upstream product

• 95-46-5 2-methylphenyl bromide 
• 1517-82-4 (-)-menthyl p-toluenesulfinate 
• 932-31-0 ortho-tolylmagnesium bromide 

Downstream Products

• 10381-68-7 1-methyl-4-(2-toluenesulfinyl)benzene 
• 794525-94-3 (S)-1-[2-(p-tolylsulfinyl)phenyl]propan-2-one 
• 794525-95-4 (S)-1-[2-(p-tolylsulfinyl)phenyl]pentan-2-one 
• 794525-97-6 (S)-1-phenyl-2-[2-(p-tolylsulfinyl)phenyl]ethan-1-one 
• 794525-98-7 (S)-2-[2-(p-tolylsulfinyl)phenyl]acetaldehyde 
• 794525-96-5 (S)-3-methyl-1-[2-(p-tolylsulfinyl)phenyl]butan-2-one 
• 835626-63-6 (S)-1-propyl-2-(p-tolylsulfinyl)benzene 
• 835626-66-9 1,2-Dimethoxy-4-{3-[2-((S)-toluene-4-sulfinyl)-phenyl]-propyl}-benzene 
• 835626-69-2 (S)-{3-[2-(p-tolylsulfinyl)phenyl]propoxy}triisopropylsilane 
• 835626-64-7 (S)-1-(2-phenylethyl)-2-(p-tolylsulfinyl)benzene 
• 100-42-5 styrene 
• 835626-65-8 C₂₂H₂₂OS 
• 835626-67-0 C₁₇H₁₈OS 
• 302934-10-7 (S)-1-ethyl-2-(p-tolylsulfinyl)benzene 

Relevant academic research and scientific papers

Synthesis of enantiomerically pure 1,2-disubstituted 2-selenoamines

Optically pure phenylseleno-(S)-2-p-tolylsulfinylbenzylcarbanions react with (S)-N-2-p-tolylsulfinylimines derived from aliphatic and aromatic aldehydes in a highly stereoselective manner affording bis-sulfinylselenoamines, easily transformed into 1-pheny