426827-01-2

Upstream product

• 426826-08-6 (3aR,4S,7S,7aR)-4,7-Bis-(4-methoxy-benzyloxy)-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxole 
• 824-94-2 p-methoxybenzyl chloride 
• 37031-29-1 (+)-dimethyl-2,3-O-isopropylidene-D-tartrate 
• 57-10-3 1-hexadecylcarboxylic acid 
• 426826-11-1 D-1-O-allyl-3,6-di-O-p-methoxybenzyl-4,5-O-isopropylidene-myo-inositol 
• 426826-05-3 (4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-(methoxy-methyl-amide) 
• 371155-65-6 (3aR,4S,7S,7aR)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 
• 175166-58-2 (S)-1-[(4R,5R)-5-((S)-1-Hydroxy-allyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-prop-2-en-1-ol 

Relevant academic research and scientific papers

Stereoselective synthesis of myo-inositol via ring-closing metathesis: a building block for glycosylphosphatidylinositol (GPI) anchor synthesis.

Here we report a concise stereoselective synthesis of myo-inositol via ring-closing metathesis. A readily available bis-Weinreb amide of D-tartrate served as a key intermediate. [reaction: see text]