140887-18-9

Upstream product

• 140887-04-3 (+/-)-2,5,6-Tri-O-benzyl-3,4-O-isopropylidene-1-O-p-methoxybenzyl-myo-inositol 
• 140887-11-2 C₄₀H₄₄O₆ 
• 140887-12-3 (+/-)-1,2,4,5-Tetra-O-benzyl-3,6-di-O-(cis-prop-1-enyl)-myo-inositol 
• 824-94-2 p-methoxybenzyl chloride 
• 134039-21-7 (+/-)-2,3,5,6-Tetra-O-benzyl-1-O-p-methoxybenzyl-myo-inositol 
• 1207481-29-5 (+)-1D-2,3,5,6-tetra-O-benzyl-1-O-(4'-methoxybenzyl)-myo-inositol 
• 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 
• 140887-13-4 (+/-)-1,2,4,5-Tetra-O-benzyl-myo-inositol 
• 141193-60-4 1D-2,3,5,6-Tetra-o-benzyl-myo-inositol 
• 140887-06-5 Bis-(-)-ω-camphanate of 1D-2,5,6-tri-O-benzyl-1-O-p-methoxybenzyl-myo-inositol 
• 140886-98-2 1D-2,3,5,6-Tetra-O-benzyl-1,4-di-O-<(+)-ω-camphanoyl>-myo-inositol 
• 111446-91-4 (+/-)-1,6-O-isopropylidene-2,4,5-tri-O-benzyl-myo-inositol 
• 115072-68-9 racemic 1,4-di-O-allyl-myo-inositol 

Relevant academic research and scientific papers

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