219776-38-2

Upstream product

• 219776-34-8 (2R,3R,4R,5S)-3,4-epoxy-2-(p-tolylsulfonyl)-5-vinyl-tetrahydrofuran-2-methanol 
• 219776-33-7 (+)-(2R,3R,4R,5S,S_S)-3,4-epoxy-4-(p-tolylsulfinyl)-5-vinyl-tetrahydrofuran-2-methanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 873438-17-6 tert-Butyl-diphenyl-[(1R,2R,4S,5R)-5-(toluene-4-sulfonyl)-4-vinyl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethoxy]-silane 
• 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 

Downstream Products

• 873438-15-4 (-)-(1S,5S,7S)-7-(tert-butyldiphenylsilyloxymethyl)-2,6-dioxabicyclo[3.3.0^4,8]octan-3-ol 

Relevant academic research and scientific papers

Reductive cleavage of tetrahydrofuryl sulfur-substituted oxiranes: Application to the formal synthesis of Kumausyne and Kumausallene

Readily available sulfnyl and sulfonyl tetrahydrofuran methanol derivatives have been transformed efficiently into a variety of substituted tetrahydrofuryl alcohols by treatment with (PhSe)2 in the presence of an excess of NaBH4. Alt