4399-34-2

Upstream product

• 860560-67-4 2-methyl-1,1-di(p-tolyl)propan-1-ol 
• 24686-79-1 4,4'-dimethyl-thiobenzophenone S-oxide 
• 51751-71-4 1-methyl-4-(propane-2-sulfonyl)benzene 
• 78752-74-6 3,3-dimethyl-4,4-bis-(p-tolyl)-1,2-oxathietan 2-oxide 
• 78752-72-4 2-hydroxy-1,1-dimethyl-2,2-bis-(p-tolyl)ethyl t-butyl sulphoxide 
• 119888-61-8 2,2-di-p-tolyl-3,3,4,4-tetramethyloxetane 
• 119888-60-7 2,2-di-p-tolyl-3,3,4-trimethyloxetane 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 4294-57-9 para-methylphenylmagnesium bromide 

Downstream Products

• 101743-00-4 2,2-dimethyl-3,3-di-p-tolyl-oxirane 
• 62897-96-5 2-methyl-1,1-di-p-tolyl-propane 

Relevant academic research and scientific papers

Organic Photochemical Reactions. XXXII. Photochemical Ring-Cleavage Reactions of 2,2-Diaryloxetanes in the Presence of Electron Donor

Photochemical ring-cleavage reactions of 2,2-diaryloxetanes in the presence of triethylamine gave 1,1-diarylethenes selectively.

Preparation of Stable β-Sultines. Crystal Structure of 2,2-Bis-(p-fluorophenyl)-3,3-dimethyl-1,2-oxathietan 2-Oxide

Three 4,4-diaryl-3,3-dimethyl-1,2-oxathietan 2-oxides were prepared by the oxidative cyclisation of 2-hydroxyalkyl t-butyl sulphoxides.They decomposed readily to 1,1-diaryl-2-methylprop-1-enes, but two of them were isolated in crystalline form.The determi

Thiophilic additions of functionalized carbanions to sulfines

The reaction of three types of sulfines with functionalized carbanions is described.Di-p-tolylsulfine 1 reacts with excess of MeSOCH2Na at the sulfine sulfur atom (thiophilic addition) to give Tol2CHS(O)CH2SOMe (Tol = p-MeC6H4).Similarly, acetonitrile wit