131233-63-1

Upstream product

• 131233-69-7 3,4,5-tri-O-benzyl-D-myo-inositol 
• 77-76-9 2,2-dimethoxy-propane 
• 100-39-0 benzyl bromide 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 
• 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 
• 131146-93-5 (+/-)-1,5,6-tri-O-benzyl-myo-inositol 
• 131147-09-6 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 131146-89-9 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol 

Downstream Products

• 131233-64-2 3,4,5,6-tetra-O-benzyl-1,2-isopropylidene-sn-myo-inositol 
• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 261722-84-3 1,3,4,5-Tetra-O-benzyl-D-myo-inositol 
• 1186371-24-3 C₃₃H₃₈O₆ 
• 1251944-12-3 C₄₉H₅₅NO₁₃ 
• 1251944-14-5 C₅₀H₅₄F₃NO₁₃ 
• 1251944-13-4 C₄₉H₅₄FNO₁₃ 
• 1251944-11-2 C₅₀H₅₇NO₁₄ 
• 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 

Relevant academic research and scientific papers

Efficient syntheses of chiral myo-inositol derivatives-key intermediates in glycosylphosphatidylinositol (GPI) syntheses

A facile and effective method was developed for large-scale syntheses of myo-inositol derivatives with the 1,2,6-O-positions differentiated from each other and from other positions as well. The syntheses started from methyl α-d-glucopyranoside, and the ke

Synthesis of optically active myo-inositol derivatives starting from phytic acid

Phytic acid treated with Baker's yeast gave D-myo-inositol-1,2,6-tris(phosphate) (α-trinositol) which was transformed into (+)-D-1,2-O-isopropylidene-myo-inositol and (-)-D-4,5-tri- O-benzyl-myo-inositol, two key intermediates in the synthesis of optically active myo-inositol derivatives and related compounds.

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