1410935-75-9

Upstream product

• 760978-01-6 endo-3-benzyloxy-endo,endo-2,4-dimethyl-8-oxabicyclo-[3.2.1]-octan-6-one 
• 171231-72-4 endo-3-benzyloxy-endo,endo-2,4-dimethyl-exo-6-hydroxy-8-oxabicyclo[3.2.1]octane 
• 171231-75-7 endo-3-benzyloxy-endo,endo-2,4-dimethyl-6,9-dioxabicyclo[3.2.1]non-7-one 
• 1410935-64-6 (2R,3R,4S,5R,6R)-5,7-bis(benzyloxy)-3-hydroxy-2,4,6-trimethyl-heptyl 4-methylbenzenesulfonate 
• 1410935-73-7 (2R,3R,4R,6R)-1,3-bis(benzyloxy)-2,4,6-trimethylnonan-5-one 
• 1410935-69-1 (2R,3R,4S,5R,6R)-1,3-bis(benzyloxy)-2,4,6-trimethylnonan-5-ol 
• 1410935-68-0 [(2R,3R,4R,5R,6R)-1,3-bis(benzyloxy)-2,4,6-trimethylnonan-5-yloxy]-tert-butyldimethylsilane 
• 1410935-67-9 (2R,3R,4S,5R,6R)-5,7-bis(benzyloxy)-3-(tert-butyldimethylsilyloxy)-2,4,6-trimethylheptyl 4-methylbenzenesulfonate 
• 1410935-60-2 (4R,5R)-4-[(2R,3R,4R)-3,5-bis(benzyloxy)-4-methylpentan-2-yl]-2,2,5-trimethyl-1,3-dioxane 
• 928840-58-8 (2R,3R,4S,5R,6R)-5,7-bis(benzyloxy)-2,4,6-trimethylheptane-1,3-diol 

Relevant academic research and scientific papers

Total synthesis of (-)-invictolide

A convergent approach to the total synthesis of (-)-invictolide, a component of the queen recognition pheromone of Solenopsis invicta, is described. Key steps involve the desymmetrization of a bicyclic olefin with Brown's chiral hydroboration, C-C bond fo