1027013-39-3

Upstream product

• 6267-39-6 3-ethoxy-5,5-dimethyl-2-cyclohexen-1-one 
• 134510-70-6 (S)-3-(tert-butyldimethylsilyloxy)-1-butyl iodide 

Downstream Products

• 189511-40-8 (S)-6-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-butyl]-1,5,5-trimethyl-cyclohex-2-enol 
• 189511-43-1 (R)-6-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-butyl]-1,5,5-trimethyl-cyclohex-2-enol 
• 189511-37-3 6-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-butyl]-5,5-dimethyl-cyclohex-2-enone 
• 41678-32-4 (-)-dihydroedulan II 

Relevant academic research and scientific papers

Chiral syntheses of edulans I, II and dihydroedulans I, II and absolute cenfigurations of edulans I, II

Enantiospecific syntheses of (+)- and (-)-edulans I, II and (-)-dihydroedulans I, II, starting from (R)- and (S)-3-hydroxybutyric acid methyl esters, allowed the determination of the absolute configurations of edulans I, II.