140887-04-3

Upstream product

• 111446-91-4 (+/-)-1,6-O-isopropylidene-2,4,5-tri-O-benzyl-myo-inositol 
• 824-94-2 p-methoxybenzyl chloride 
• 100-39-0 benzyl bromide 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 
• 98906-30-0 (+/-)-2,5,6-tri-O-benzyl-myo-inositol 

Downstream Products

• 136091-46-8 (+/-)-2,4,5-Tri-O-benzyl-1-O-p-methoxybenzyl-myo-inositol 
• 141040-54-2 (+)-2,5,6-tri-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 
• 226889-48-1 (1S,2S,3R,4S,5S,6S)-3,4,6-Tris-benzyloxy-5-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 180794-83-6 (-)-2,4,5,6-tetra-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 3-(dibenzyl phosphate) 
• 187841-49-2 Phosphorous acid dibenzyl ester (1S,2R,3S,4S,5S,6S)-2,3,5-tris-benzyloxy-6-(bis-benzyloxy-phosphanyloxy)-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 180979-80-0 (+)-2,5,6-tri-O-benzyl-myo-inositol 3,4-bis(dibenzyl phosphate) 
• 180979-79-7 (-)-2,5,6-tri-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 3,4-bis(dibenzyl phosphate) 
• 141040-56-4 (+)-2,4,5,6-tetra-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 
• 187979-52-8 1D-2,4,5,6-tetra-O-benzyl-3-O-(4'-methoxybenzyl)-myo-inositol 
• 180794-82-5 (+)-3-O-allyl-2,4,5,6-tetra-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 
• 187841-22-1 1D-1-O-allyl-2,4,5,6-tetra-O-benzyl-3-O-p-methoxybenzyl-myo-inositol 
• 187841-23-2 1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene 
• 115509-76-7 (-)-1D-2,5,6-tri-O-benzyl-myo-inositol 
• 140887-15-6 (+/-)-1,2,4,5-Tetra-O-benzyl-myo-inositol 3,6-bis 

Relevant academic research and scientific papers

The preparation of racemic and enantiomerically pure myo-inositol derivatives as intermediates for the synthesis of phosphatidylinositol 3-, 3,4-bis-, and 3,4,5-tris-phosphates and for the synthesis of analogues of 1D-myo-inositol 1,3,4,5-tetrakisphosphat

Details of the products obtained by the tin-mediated allylation and benzylation of 1,2-O-isopropylidene-myo-inositol, which were previously described in a preliminary communication, are provided here. Some of the products from these reactions, particularl

The preparation, resolution, and phosphorylation of some benzyl ethers of myo-inositol: Intermediates for the synthesis of myo-inositol phosphates of the phosphatidylinositol cycle

The syntheses of the following chiral compounds are described: 1D-2,3,6-tri-, 1D-2,4,5-tri, 1D-2,5,6-tri-, 1D-1,2,3,4-tetra, 1D-1,2,3,6-tetra-, 1D-1,2,4,5-tetra-, and 1D-2,3,5,6-tetra-0-benzyl-myo-inositol; and 1D-2,5,6-tri-0-benzyl-1-0-p-methoxybenyl- an