69690-06-8

Upstream product

• 69690-05-7 2-Methyl-2-phenylsulfanyl-but-3-enal 
• 103697-38-7 2-acetoxy-2-methyl-1-phenylsulfinylbut-3-ene 
• 57282-70-9 (E)-4-hydroxy-3-methyl-2-butenyl phenyl sulfide 

Downstream Products

• 1606991-83-6 (E)-1,1-dimethyl-2-[(E)-2-methyl-4-(phenylthio)but-2-enylidene]hydrazine 
• 1606991-73-4 (E)-3-[(E)-(2,2-dimethylhydrazono)methyl]-3-methyl-5-(phenylthio)pent-4-en-2-ol 
• 1606991-69-8 (E)-5,5-dimethyl-2-[4-(phenylthio)but-2-en-2-yl]-1,3-dioxane 
• 121783-39-9 (E)-2-methyl-4-(phenylsulfonyl)but-2-enal 

Relevant academic research and scientific papers

Ruthenium-catalysed Oxidation of Allyl Alcohols by Molecular Oxygen

Ruthenium(II) catalyses the homogeneous oxidation of allyl alcohols to carbonyl compounds by molecular oxygen under mild conditions.

Reactions of α-or χ-Phenylthio Substituted Extended Enolate Anions Derived from Esters

The title anions are alkylated and acylated (α series only) exclusively at the α position.The α-phenylthio products give χ-phenylthio compounds by the PhS shift and the PhS group may be removed from the products in a number of ways.