111420-50-9

Upstream product

• 111392-10-0 (+/-)-1,2:4,5-di-O-isopropylidene-3,6-di-O-p-methoxybenzyl-myo-inositol 
• 142387-37-9 2,5-di-O-p-methoxybenzyl-myo-inositol 
• 77-76-9 2,2-dimethoxy-propane 
• 824-94-2 p-methoxybenzyl chloride 
• 142387-35-7 C₃₄H₄₄O₈ 
• 136986-12-4 1,3,4,6-tetra-O-allyl-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 

Downstream Products

• 162879-74-5 1D-1,3,6-tri-O-benzyl-2,5-di-O-p-methoxybenzyl-myo-inositol 
• 162991-61-9 (1S,2S,3S,4S,5S,6R)-4,5-Bis-benzyloxy-3,6-bis-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 162991-32-4 (1R,2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-3,6-bis-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 162879-71-2 bis-(-)-ω-camphonate of 1,6-di-O-benzyl-2,5-di-O-p-methoxybenzyl-myo-inositol 
• 162991-31-3 bis-(-)-ω-camphonate of 1,6-di-O-benzyl-2,5-di-O-p-methoxybenzyl-myo-inositol 
• 162991-62-0 (3aR,4S,5S,6R,7S,7aR)-4,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-5-ol 
• 98906-30-0 (±)-1,3,6-tri-O-benzyl-myo-inositol 
• 111392-16-6 1,4,5-tri-O-allyl-2,3,6-tri-O-p-methoxybenzyl-myo-inositol 
• 111392-17-7 1,2,4-tri-O-p-methoxybenzyl-myo-inositol 
• 111392-13-3 1,4,5-tri-O-allyl-3,6-di-O-p-methoxybenzyl-myo-inositol 
• 111392-12-2 5,6-di-O-allyl-1,4-di-O-p-methoxybenzyl-myo-inositol 
• 111392-11-1 (3aR,4R,5S,6S,7R,7aS)-5,6-Bis-allyloxy-4,7-bis-(4-methoxy-benzyloxy)-2,2-dimethyl-hexahydro-benzo[1,3]dioxole 

Relevant academic research and scientific papers

The preparation and phosphorylation of 2,5- and 1D-2,6-di-O-benzyl-myo-inositol

1,3,4,6-Tetra-O-allyl-myo-inositol was converted into the 2,5-di-O-benzyl- and 2,5-di-O-p-methoxybenzyl ethers, and the products were deallylated to give the 2,5-di-O-benzyl (and p-methoxybenzyl) ethers of myo-inositol, which were converted into the mono-

The Allyl Group for Protection in Carbohydrate Chemistry. Part 18. Allyl and Benzyl Ethers of myo-Inositol. Intermediates for the Synthesis of myo-Inositol Triphosphates

Racemic 1,2:4,5-di-O-isopropylidene-myo-inositol was converted into racemic 1,2,4-tri-O-benzyl-myo-inositol, 1,2,4-tri-O-p-methoxybenzyl-myo-inositol and 2,4,5-tri-O-benzyl-myo-inositol using allyl groups for 'temporary' protection.The benzyl ethers are required as intermediates for the synthesis of the 'second messenger', inositol 1,4,5-triphosphate and its metabolite, inositol 1,3,4-triphosphate. 1,2,3,4-Tetra-O-benzyl-myo-inositol, and its two monoallyl and monoprop-1-enyl ethers, were also prepared as model compounds for phosphorylation studies of the vicinal 5,6-diol system which occurs in 1,2,4-tri-O-benzyl-myo-inositol.