936650-20-3

Upstream product

• 17049-50-2 n-decyl magnesium bromide 
• 936650-19-0 (4S,5S)-4,5-bis((R)-1-hydroxyundec-1-yl)-2,2-dimethyl-1,3-dioxolane 
• 936650-18-9 (4R,5R)-4,5-diundecanoyl-2,2-dimethyl-1,3-dioxolane 

Downstream Products

• 85514-80-3 (R)-2-(benzyloxy)dodecanal 
• 936650-21-4 (4R,5R)-5-(benzyloxy)pentadec-1-en-4-ol 
• 936650-22-5 (4R,5R)-5-(benzyloxy)-4-(p-toluenesulfonyloxy)pentadec-1-ene 
• 936650-23-6 (7R,8R)-8-(benzyloxy)-7-(p-toluenesulfonyloxy)-2-methyloctadec-4-ene 
• 936650-24-7 (4R,5R)-5-(benzyloxy)-4-(tert-butyldimethylsilyloxy)pentadec-1-ene 
• 936650-26-9 (11R,12R)-12-(tert-butyldimethylsilyloxy)-17-methyloctadecan-11-yl-4-methylbenzenesulfonate 
• 54910-51-9 (2S-cis)-7,8-epoxy-2-methyloctadecane 
• 105243-14-9 (7R,8R)-(+)-8-hydroxy-7-p-toluenesulfonyloxy-2-methyloctadecane 

Relevant academic research and scientific papers

Enantiodivergent synthesis of both enantiomers of gypsy moth pheromone disparlure

(Chemical Equation Presented) Enantiodivergent synthesis of both (-)- and (+)-disparlure, a bioactive pheromone, possessing a cis-epoxide has been accomplished. The key step involves the cross metathesis of a chiral homoallylic alcohol derived from L-(+)-tartaric acid.