99894-19-6

Upstream product

• 32501-94-3 (ethynylsulfonyl)benzene 
• 71242-58-5 (1S,2R,4R)-(-)-10-mercaptoisoboneol 
• 21286-54-4 Camphorsulfonyl chloride 

Downstream Products

• 99894-24-3 (1S,2R,4R)-1-((R)-(1S,2R,3S,4R)-3-Benzenesulfonyl-bicyclo[2.2.1]hept-5-ene-2-sulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 103953-47-5 (1S,4R,6R,8R)-4-Benzenesulfonylmethyl-11,11-dimethyl-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane 
• 103953-51-1 (1S,4R,6R,8R)-4-Benzenesulfonylmethyl-11,11-dimethyl-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane 3,3-dioxide 
• 103953-50-0 (1S,4R,6R,8R)-4-Benzenesulfonylmethyl-11,11-dimethyl-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane 3-oxide 
• 100946-62-1 (1S,2R,4R)-1-((E)-2-Benzenesulfonyl-ethenesulfonylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 101052-88-4 (1S,2R,4R)-1-((R)-(E)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 101052-89-5 (1S,2R,4R)-1-((S)-(E)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 100946-61-0 (1S,2R,4R)-1-((Z)-2-Benzenesulfonyl-ethenesulfonylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 99946-17-5 (1S,2R,4R)-1-((S)-(Z)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 99894-21-0 (1S,2R,4R)-1-((R)-(Z)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 104012-54-6 (1S,2R,4R)-1-((Z)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 103953-47-5 (1S,4S,6R,8R)-4-Benzenesulfonylmethyl-11,11-dimethyl-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane 
• 100946-58-5 (1S,2R,4R)-1-((E)-2-Benzenesulfonyl-vinylsulfanylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 
• 99894-21-0 1-((Z)-2-Benzenesulfonyl-ethenesulfinylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol 

Relevant academic research and scientific papers

Asymmetric Diels-Alder Reactions of Sulphinyl-activated Dienophiles obtained via a Self-induced Chiral Oxidation

The Diels-Alder cycloaddition of activated vinyl sulphoxides (1), that are readily obtained by a self-induced chiral oxidation, proceeds highly diastereoselectively to form the corresponding cycloadducts (4) that can be converted into 2-substituted norbor

Self-Induced Diastereoselective Oxidation of Vinyl Sulfides Bearing a Chiral Hydroxy Group as a Way of Preparation of Optically Active Sulfinyl Dienophiles and Their Use in the Asymmetric Diels-Alder Reaction to Cyclopentadiene

Dienophiles 4,5,4' and 5' add with excellent diastereoselectivity to cyclopentadiene as a result of the fact that they assembled most features that are known to govern facial selectivity.Their synthesis entails stereoselective Michael addition of hydroxyt

CHIRAL 1,3-OXATHIANES VIA STEREOSELECTIVE ADDITION-CYCLIZATION OF HYDROXYTHIOLS TO ELECTRON-POOR ACETYLENES

A novel preparation of chiral 1,3-oxathianes via nucleophilic addition of hydroxythiols to electron-poor acetylenes, followed by iodine catalyzed photoinduced cyclization is reported.The stereochemical outcome of the reaction is determined with a conforma