106918-89-2

Upstream product

• 61173-91-9 1-phenyl-2-(phenylthio)-1-butene 
• 111198-12-0 1-(2-phenyl-1-phenylthioethyl)benzotriazole 
• 111198-03-9 1-((phenylthio)methyl)-1H-benzo[d][1,2,3]triazole 
• 100-39-0 benzyl bromide 

Downstream Products

• 115993-69-6 2-Benzyl-2-phenylsulfanyl-butyronitrile 
• 106918-98-3 2-(1-Benzyl-1-phenylsulfanyl-propyl)-cyclohexanone 

Relevant academic research and scientific papers

One electron transfer reaction of phenyl vinyl sulfides with dioxygen. The fate of the intermediate vinyl sulfide radical cations

Mild reaction of phenyl vinyl sulfides with dioxygen can lead to the eventual formation of rearranged vinyl sulfides and/or carbonyl-containing sulfide products, which are believed to result from decomposition of initially-formed vinyl sulfide radical cations. Supporting evidence is provided by the comparable findings obtained from the one electron oxidation of one vinyl sulfide by cerium (IV) ammonium nitrate.

182. A Convenient Synthesis of Vinyl Sulfides

tert-Alkyl sulfides, with an α-(1H-benzotriazol-1-yl) group 6 and 13, are readily prepared from N--1H-benzotriazoles 3 and N-(11), respectively, by reaction with BuLi and then with the appropriate electrophile.The tert-alkyl sulfides 6 a