87184-65-4

Upstream product

• 285-67-6 Cyclopentene oxide 
• 106-45-6 para-thiocresol 
• 84613-02-5 2-(p-tolylthio)cyclopentanone 
• 103-19-5 di(p-tolyl) disulfide 
• 120-92-3 cyclopentanone 

Downstream Products

• 87184-66-5 trans-2-((4-methylphenyl)sulfonyl)cyclopentanol 
• 91767-59-8 (+/-)-trans-1-chloro-2-(toluene-4-sulfonyl)-cyclopentane 
• 87184-73-4 t-2-methyl-2-((4-methylphenyl)sulfonyl)-r-cyclopentanol 
• 87184-71-2 c-2-methyl-2-((4-methylphenyl)sulfonyl)-r-1-cyclopentanol 
• 87184-72-3 2-methyl-2-((4-methylphenyl)sulfonyl)cyclopentanone 
• 87184-68-7 α-(p-methylbenzenesulfonyl)cyclopentanone 
• 87184-69-8 cis-2-((4-methylphenyl)sulfonyl)cyclopentanol 
• 91767-80-5 trans-1-chloro-2-(p-tolylsulfenyl)cyclopentane 

Relevant academic research and scientific papers

An efficient catalyst for ring opening of epoxides with phenol and thiophenol under solvent-free conditions

An efficient and rapid procedure for ring opening reaction of various epoxides with phenol and thiophenol derivatives was developed. The procedure can be obtained at room temperature under solvent-free condition in presence of (C4H12N2)2[BiCl6] Cl·H2O (1 mol %). This catalyst can be reused several times without significant loss of activity.

Convenient preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium into chalcogen-chalcogen bonds. Application in the ring-opening of epoxides

Convenient conditions are reported for the preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium metal into the chalcogen- chalcogen bond of disulfides, diselenides, and ditellurides. The resulting complexes have been found to t

Preparation and Stereochemistry of Methylation of Some Cycloalkyl Sulfones

3-((4-methylphenyl)sulfonyl)cyclohexanols (2, 3), 3-((4-methylphenyl)sulfonyl)cyclopentanols (7, 8), and 2-((4-methylphenyl)sulfonyl)cyclopentanols (12, 15) and their tetrahydropyranyl ether derivatives were prepared.Attempted methylation of the tetrahydr