34220-15-0

Upstream product

• 57557-60-5 3-methyl-2-(phenylthio)butanoic acid 
• 101518-51-8 3-Methyl-2-phenylsulfanyl-butyric acid ethyl ester 
• 108-64-5 Ethyl isovalerate 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 34220-16-1 3,5-Dinitro-benzoic acid 2-benzenesulfonyl-3-methyl-butyl ester 
• 34224-40-3 3-Methyl-2-phenylthiobutyl-phenylsulfid 
• 66165-02-4 2-Butoxy-3-methylbutyl-phenylsulfid 
• 132331-33-0 (S/R)-2-(phenylsulfanyl)-3-methylbutanal 
• 711028-31-8 (E)-6-Methyl-5-phenylsulfanyl-hept-3-en-2-one 

Relevant academic research and scientific papers

Do the electronic effects of sulfur indeed control the π-selectivity of γ-sulfenyl enones? An investigation

The electronic effects of sulfur in γ-sulfenyl enones are not transmitted to the carbonyl carbon through the π bond as reported previously. The diastereoselectivity is rather controlled by a combination of several other factors. The steric effects arising

Scope and limitations of allyl sulphide synthesis by [1,2] and [1,3] phenylthio migration

β-Phenylthio-alcohols rearrange in acidic solution (toluene-p-sulphonic acid in benzene under reflux) to give allyl sulphides by phenylthio migration. High yields of single products useful in organic synthesis are obtained with a tertiary or secondary mig