78086-90-5

Upstream product

• 498-66-8 norborn-2-ene 
• 106-45-6 para-thiocresol 
• 61376-30-5 exo-3-p-tolylsulfenylnorbornan-exo-2-ol 
• 61376-28-1 exo-3-p-tolylsulfenylnorbornan-endo-2-ol 
• 78019-35-9 (1S,3S,4R)-3-((S)-Toluene-4-sulfinyl)-bicyclo[2.2.1]heptan-2-one 
• 78019-32-6 (1S,2R,3S,4R)-3-((S)-Toluene-4-sulfinyl)-bicyclo[2.2.1]heptan-2-ol 

Downstream Products

• 61348-91-2 3-(p-Tolylsulfonyl)norbornan-2-one 
• 61376-34-9 3-exo-(p-Tolylsulfonyl)-2-endo-norbornanol 
• 78019-35-9 (1S,3S,4R)-3-((S)-Toluene-4-sulfinyl)-bicyclo[2.2.1]heptan-2-one 
• 78019-32-6 (1S,2R,3S,4R)-3-((R)-Toluene-4-sulfinyl)-bicyclo[2.2.1]heptan-2-ol 
• 78019-32-6 (1S,2S,3S,4R)-3-((S)-Toluene-4-sulfinyl)-bicyclo[2.2.1]heptan-2-ol 
• 61376-28-1 exo-3-p-tolylsulfenylnorbornan-endo-2-ol 
• 78019-35-9 3-(p-Tolylsulfoxyl)norbornan-2-one 

Relevant academic research and scientific papers

Hydroxy Sulfoxides Derived from Norbornene: Determination of Stereochemistry, and Synthesis by Stereoselective Oxidation

The structure (5) of one of the hydroxy sulfoxides formed by thiol-oxygen cooxidation of norbornene has been determined by X-ray diffraction.Other products have been related to it by appropriate chemical transformations.The stereospecific, or highly stere

Thiol-Oxygen Cooxidation Reactions of Cyclopentene, cis- and trans-But-2-ene, Norbornene, and Norbornadiene

Thiol-oxygen cooxidation (TOCO) of olefins, followed by reduction of the initially formed hydroperoxides with triphenylphosphine, affords β-hydroxy sulfides in moderate to good yields.The structures of the major products from cis- and trans-but-2-ene and