848784-50-9

Upstream product

• 31350-91-1 (R)-chloromethyl p-tolyl sulfoxide 
• 848784-38-3 (R)-(E)-1-chloro-4-phenyl-1-(p-tolylsulfinyl)-1-butene 
• 848784-32-7 1-Chloro-4-phenyl-1-((R)-toluene-4-sulfinyl)-butan-2-ol 
• 104-53-0 3-phenyl-propionaldehyde 
• 848784-43-0 tert-butyl (-)-[3-chloro(p-tolylsulfinyl)methyl]-5-phenylpentanoate 

Downstream Products

• 848784-52-1 tert-butyl (S)-(-)-3-methyl-5-phenylpentanoate 
• 41927-32-6 (S)-(-)-3-methyl-5-phenylpentanoic acid 

Relevant academic research and scientific papers

Asymmetric synthesis of both enantiomers of esters and γ-lactones from optically active 1-chlorovinyl p-tolyl sulfoxides and lithium ester enolates with the formation of a tertiary or a quaternary carbon stereogenic center at the β-position

Treatment of optically active 1-chlorovinyl p-tolyl sulfoxides having two different substituents at the 2-position, which were synthesized from aldehydes or unsymmetrical ketones and (R)-(-)-chloromethyl p-tolyl sulfoxide in two or three steps, with the l