219776-33-7

Upstream product

• 219776-31-5 (-)-(4E)-(3S,S_S)-4-(p-tolylsulfinyl)hepta-1,4,6-trien-3-ol 
• 219776-32-6 (+)-cis-4-(p-tolylsulfinyl)-5-vinyl-2,5-dihydrofuran-2-methanol 
• 219776-30-4 (+)-(4E)-(3R,S_S)-4-(p-tolylsulfinyl)hepta-1,4,6-trien-3-ol 
• 951133-73-6 (R)-(1,3-Butadienyl)-p-tolyl-sulfoxid 

Downstream Products

• 219776-34-8 (2R,3R,4R,5S)-3,4-epoxy-2-(p-tolylsulfonyl)-5-vinyl-tetrahydrofuran-2-methanol 
• 873438-45-0 tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-((S)-toluene-4-sulfinyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane 
• 873438-15-4 (-)-(1S,5S,7S)-7-(tert-butyldiphenylsilyloxymethyl)-2,6-dioxabicyclo[3.3.0^4,8]octan-3-ol 
• 219776-38-2 (+)-(2S,4S,5S)-2-(tert-butyldiphenylsilyloxymethyl)-5-vinyltetrahydrofuran-4-ol 

Relevant academic research and scientific papers

Nucleophilic epoxidation of α′-hydroxy dienyl sulfoxides

A novel route to enantiopure densely functionalized epoxy sulfinyl tetrahydrofurans, based on the unexpected and highly stereoselective remote nucleophilic epoxidation of hydroxy 1-sulfinyl butadienes with t-BuOOK, followed by ring closure and subsequent