89002-90-4

Upstream product

• 115125-55-8 3-(p-tolylthio)cyclohexene 
• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 37488-68-9 1-(cyclohex-2-en-1-ylsulfonyl)-4-methylbenzene 
• 917-54-4 methyllithium 
• 1227872-34-5 3-methylcyclohex-2-enyl toluene-p-sulphinate 

Downstream Products

• 89003-00-9 3-methylcyclohex-2-enyl p-tolyl sulphone 
• 120801-59-4 4-methyl-4-p-tolylsulphonylcyclohex-2-enyl (3'-p-tolylsulphonyl)propionate 
• 120801-52-7 4-methyl-4-p-tolylsulphonylcyclohex-2-enyl 2'-trimethylsilylacrylate 
• 120801-56-1 5-Methyl-3-[1-(toluene-4-sulfonyl)-ethyl]-2,3,3a,6,7,7a-hexahydro-benzofuran 
• 120801-50-5 4-methyl-4-p-tolylsulphonylcyclohex-2-enyl acrylate 
• 120801-49-2 4-methyl-4-p-tolylsulphonylcyclohex-2-enyl but-2-enyl ether 
• 99285-69-5 4-methyl-4-p-tolylsulphonylcyclohex-2-enyl allyl ether 
• 120801-60-7 4-methyl-4-p-tolylsulphonylcyclohex-2-en-1-ol 
• 99285-70-8 3-methyl-9-p-tolylsulphonylmethyl-7-oxabicyclo<4.3.0>non-2-ene 
• 120801-46-9 1-bromo-4-methyl-4-p-tolylsulphonylcyclohex-2-ene 

Relevant academic research and scientific papers

Preparation of some Allylic Sulphones; Base-catalysed Isomerisation and Deuteriation of Cyclohex-2-enyl p-Tolyl Sulphones

A summary of the methods used in the preparation of a range of allylic sulphones is given.In the case of the conformationally biased sulphones (5) and (6) stereospecific preparation from the cis- and trans-5-t-butylcyclohex-2-en-1-ols was achieved by rear

Rearrangement of Some Allylic Sulphinate Esters to Allylic Sulphones. Ion-pair and Sigmatropic Shift Mechanisms

The mechanism of rearrangement of a number of allylic sulphinate esters to the corresponding allylic sulphones on heating in formamide has been investigated as a function of substrate structure.Simple systems such as crotyl and α-methylallyl-sulphinate ap