155366-43-1

Upstream product

• 117286-10-9 undecylmagnesium bromide 
• 74134-79-5 (4R)-2,2-dimethyl-4-[(2R)-oxiran-2-yl]-1,3-dioxolane 
• 824-94-2 p-methoxybenzyl chloride 
• 155366-42-0 (2R,3R)-1,2-O-methylethylidene-pentadecane-1,2,3-triol 

Downstream Products

• 161807-82-5 (4R,5R)-5-O-(p-methoxybenzyl)-4-heptadecanolide 
• 155366-45-3 (2R,3R)-1,2-epoxy-3-O-(p-methoxybenzyl)-3-pentadecanol 
• 155366-44-2 (2R,3R)-3-O-(p-methoxybenzyl)-pentadecane-1,2,3-triol 

Relevant academic research and scientific papers

Enantiopure hydroxylactones from L-ascorbic and D-isoascorbic acids. Part I. Synthesis of (-)-muricatacin

From D-isoascorbic acid, via a formal bis-epoxide equivalent with a C-2 axis of symmetry, two possible syntheses of the (-)-Muricatacin are described.

Synthesis of (-)-Muricatacin and -(5R,6S)-6-acetoxy-5-hexadecanolide, the Mosquito oviposition attractant pheromone, from D-isoascorbic acid

From D-isoascorbic acid, a general approach to enantiomerically pure hydroxy γ-butyro and δ-valero lactones, (-)-Muricatacin and (-)-(5R,6S)-6-acetoxy-5-hexadecanolide, via a four carbon atoms bisepoxide equivalent, is reported.