131233-72-2

Upstream product

• 131233-71-1 1D-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 106-95-6 allyl bromide 
• 100-39-0 benzyl bromide 
• 116786-69-7 (+/-)-1,6-di-O-allyl-4,5-di-O-benzyl-myo-inositol 
• 131147-01-8 (+/-)-1,6-di-O-allyl-4,5-di-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 115072-69-0 (+/-)-1,6-di-O-allyl-2,3:4,5-di-O-isopropylidene-myo-inositol 
• 131147-00-7 (3aS,4R,5R,6S,7R,7aR)-6,7-Bis-allyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,5-diol 
• 131147-10-9 4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (3aS,4S,5R,6S,7S,7aS)-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-yl ester 
• 131147-11-0 (3aR,4S,5S,6R,7S,7aS)-4-Allyloxy-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole 
• 131146-89-9 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 131233-66-4 (3aR,4S,5S,6R,7S,7aS)-5,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131147-09-6 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 131147-07-4 (+/-)-1,6-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 

Downstream Products

• 131233-73-3 1D-3,4-di-O-allyl-1,2,5,6-tetra-O-benzyl-myo-inositol 
• 131147-16-5 C₄₀H₄₄O₆ 
• 131233-74-4 2-O,3-O,4-O,5-O-tetrabenzyl-L-myo-inositol 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 6195-66-0 (+/-)-1,2,5,6-tetra-O-benzyl-myo-inositol 
• 131147-14-3 (+/-)-1,3,4,5-tetra-O-benzyl-myo-inositol 
• 131146-93-5 (+/-)-1,5,6-tri-O-benzyl-myo-inositol 

Relevant academic research and scientific papers

Dimethyltin Dichloride Catalyzed Regioselective Alkylation of cis-1,2-Diols at Room Temperature

Here, we have developed a mild and general method for the regioselective installation of benzyl, allyl, para-methoxybenzyl and naphthyl groups on cis-1,2-diols. The optimized method operates at room temperature using dimethyltin dichloride as catalyst and

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