131146-89-9

Upstream product

• 131147-09-6 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 131146-93-5 (+/-)-1,5,6-tri-O-benzyl-myo-inositol 
• 77-76-9 2,2-dimethoxy-propane 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131147-07-4 (+/-)-1,6-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 111392-27-9 (+/-)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 120679-73-4 (+/-)-3,4-di-O-benzyl-1,2:5,6-di-O-isopropylidene-myo-inositol 
• 131146-90-2 (+/-)-3-O-benzyl-1,2-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 131147-03-0 (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 38643-30-0 (±)-1,2:5,6-di-O-isopropylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 

Downstream Products

• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 131147-12-1 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol 
• 131147-13-2 1D-1,3,5,6-tetra-O-benzyl-4-O-(prop-1-enyl)-myo-inositol 
• 131233-73-3 1D-3,4-di-O-allyl-1,2,5,6-tetra-O-benzyl-myo-inositol 
• 131147-16-5 C₄₀H₄₄O₆ 
• 131233-70-0 1D-1,5,6-tri-O-benzyl-myo-inositol 
• 131233-69-7 3,4,5-tri-O-benzyl-D-myo-inositol 
• 131233-71-1 1D-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 131233-63-1 (3aS,4R,5R,6S,7R,7aR)-5,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 131233-66-4 (3aR,4S,5S,6R,7S,7aS)-5,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 131147-11-0 (3aR,4S,5S,6R,7S,7aS)-4-Allyloxy-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole 
• 131233-72-2 1,6-di-O-allyl-3,4,5-tri-O-benzyl-L-myo-inositol 
• 131233-74-4 2-O,3-O,4-O,5-O-tetrabenzyl-L-myo-inositol 

Relevant academic research and scientific papers

The alkylation of dibutylstannylene derivatives of 1,2-O-isopropylidene-myo-inositol

Benzylation (or allylation) of 1,2-O-isopropylidene-myo-inositol in the presence of an excess of dibutyltin oxide gives, as major products, the readily isolable 3,4,6- (12) and 3,5,6-tri-O-alkyl (13) derivatives which are valuable intermediates for the synthesis of inositol phosphates of the phosphates of the phosphatidylinositol cycle.

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative