924288-69-7

Upstream product

• 3761-92-0 n-hexylmagnesium bromide 
• 924288-67-5 1-[5-(1-hydroxy-heptyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-heptan-1-ol 
• 924288-66-4 1-(5-heptanoyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-heptan-1-one 
• 924288-68-6 4,5-bis-(1-benzyloxy-heptyl)-2,2-dimethyl-[1,3]dioxolane 

Downstream Products

• 118535-81-2 (S)-2-Benzyloxy-octanal 
• 675127-22-7 1-[1-benzyloxy-(1S)-heptyl]-(1S)-3-butenyl alcohol 
• 852509-25-2 (4R,5R)-4,5-dibenzyloxyhept-6-enoic acid (1'S,1''S)-1'-(1''-benzyloxyheptyl)-3'-butenyl ester 
• 852509-26-3 (5R,6R,7E,10S)-10-[(1'S)-1'-benzyloxyheptyl]-5,6-dibenzyloxy-3,4,5,6,9,10-hexahydro-2H-oxecin-2-one 

Relevant academic research and scientific papers

Stereoselective synthesis of (-)-microcarpalide

A stereoselective approach for the synthesis of the bio-active decanolactone (-)-microcarpalide was achieved from chiral pool tartaric acid. The synthesis of pivotal intermediates en route to the decanolactone was achieved from α-benzyloxy aldehydes deriv