136118-83-7

Upstream product

• 117666-30-5 (+/-)-1,3,4,5-tetra-O-allyl-2,6-di-O-benzyl-myo-inositol 
• 142387-43-7 (+/-)-2,4-di-O-benzyl-1,6-O-isopropylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 142387-45-9 (+/-)-2,6-di-O-benzyl-3,4-O-isopropylidene-1,5-di-O-p-methoxybenzyl-myo-inositol 
• 136986-14-6 (+/-)-1,3,4,5-tetra-O-allyl-myo-inositol 
• 16749-97-6 racemic 2,4-di-O-benzyl-myo-inositol 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 

Downstream Products

• 142387-47-1 C₅₆H₆₄O₁₄ 
• 142387-47-1 C₅₆H₆₄O₁₄ 
• 16749-97-6 racemic 2,4-di-O-benzyl-myo-inositol 

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 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-