71847-74-0

Upstream product

• 108-98-5 thiophenol 
• 80-62-6 methacrylic acid methyl ester 
• 1154689-97-0 methyl (E)-2-methyl-3-(p-toluenesulfonyloxy)prop-2-enoate 
• 777-80-0 methyl 3-(phenylthio)isobutyrate 

Downstream Products

• 71847-64-8 3-Methyl-2-oxo-4-phenylsulfanyl-cyclopent-3-enecarboxylic acid methyl ester 
• 71847-71-7 (E)-2,5-Dimethyl-4-oxo-3-phenylsulfanyl-hex-2-enoic acid methyl ester 
• 71847-73-9 (E)-2-Methyl-4-oxo-4-phenyl-3-phenylsulfanyl-but-2-enoic acid methyl ester 
• 71847-72-8 (E)-2,5,5-Trimethyl-4-oxo-3-phenylsulfanyl-hex-2-enoic acid methyl ester 
• 71847-70-6 (E)-2-Methyl-4-oxo-3-phenylsulfanyl-hex-2-enoic acid methyl ester 

Relevant academic research and scientific papers

ALPHA, BETA-UNSATURATED IMIDATE COMPOUND AND PESTICIDAL COMPOSITION CONTAINING THE SAME

There is provided a compound having an excellent controlling effect on pests, represented by the formula (I): wherein, A and E independently represent a -R1 group, a -L1-R1 group, etc.; G represents a -L2-R

Oxidative Functionalization of the β-Carbon in α,β-Unsaturated Systems. Preparation of 3-Phenylthio Enones, Acrylates, and Other Vinyl Derivatives

The β-carbon of α,β-unsaturated ketones, esters, lactones, and nitriles can be oxidatively functionalized in a regiospecific manner in a simple sequence of reactions.Michael addition of thiophenol followed by oxidation with N-chlorosuccinimide gives chloro sulfides that readily lose HCl to give 3-phenylthio enones, acrylates, and other vinyl derivatives.