213818-77-0

Upstream product

• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 270931-86-7 (3R,7R)-7-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-octanoic acid ethyl ester 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 71171-66-9 (3R)-3-(tert-butyldimethylsilyloxy)butanal 
• 104524-19-8 methyl (R)-(-)-3-(tert-butyldimethylsilyloxy)butyrate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 154568-30-6 (5R,2E)-5-(tert-butyl-dimethyl-silyloxy)-hex-2-enoic acid ethyl ester 
• 121785-59-9 (-)-(5R)-5-(tert-butyldimethylsilyloxy)-hexanal 
• 174419-62-6 ethyl (5R)-5-[(tert-butyldimethylsilyl)oxy]hexanoate 
• 213818-74-7 S-ethyl (R)-3-(tert-butyldimethylsiloxy)butanoate 
• 213818-76-9 S-ethyl (3R,7R)-7-(tert-butyldimethylsiloxy)-3-hydroxyoctanoate 

Downstream Products

• 213818-79-2 (3R,7R)-3-Benzyloxy-7-hydroxy-octanoic acid 
• 213818-80-5 (4R,8R)-4-Benzyloxy-8-methyl-oxocan-2-one 
• 213818-78-1 (3R,7R)-3-Benzyloxy-7-hydroxy-octanoic acid ethyl ester 

Relevant academic research and scientific papers

Determination of Relative and Absolute Stereochemistry of Cephalosporolide D and Its Enantioselective Total Synthesis

An efficient method for the synthesis of (-)-cephalosporolide D was established via successive enantioselective aldol reaction and effective construction of 8-membered ring lactone moiety.