115072-72-5

Upstream product

• 100-39-0 benzyl bromide 
• 114218-23-4 (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 114218-20-1 (+/-)-3-O-allyl-1,4-di-O-benzyl-myo-inositol 
• 114218-19-8 1-O-Allyl-2,3,6-tri-O-benzyl-4,5-O-isopropylidene-myo-inositol 

Downstream Products

• 98906-30-0 (±)-2,3,6-tri-O-benzyl-myo-inositol 
• 145508-52-7 Sulfamic acid (1R,2R,3S,4R,5R,6S)-2,3,6-tris-benzyloxy-4,5-bis-sulfamoyloxy-cyclohexyl ester 
• 111446-91-4 (+/-)-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 

Relevant academic research and scientific papers

Synthesis of analogues of myo-inositol 1,4,5-trisphosphate that contain sulfonamide, sulfate, methylphosphonate, and carboxymethyl groups

The syntheses are described of four isosteric racemic myo-inositol 1,4,5-trisphosphate (1) analogues with the phosphate groups replaced by sulfonamide (2), sulfate (3), methylphosphonate (4), and carboxymethyl (5). None of these compounds had any affinity

Synthesis of 1,4,5-trissulphated and 1,4,5-trissulphamoylated myo-inositols: Isosteric myo-inositol 1,4,5-trisphosphate analogues

Synthesis of the myo-inositol 1,4,5-trisphosphate isosteric analogues (rac.) 1,4,5-trissulphate and (rac.) 1,4,5-trissulphonamido was accomplished from 1,2,4-tri-O-benzyl myo-inositol.

THE ALLYL GROUP FOR PROTECTION IN CARBOHYDRATE CHEMISTRY. PART 21. (+/-)-1,2:5,6- AND (+/-)-1,2:3,4-DI-O-ISOPROPYLIDENE-MYO-INOSITOL. THE UNUSUAL BEHAVIOUR OF CRYSTALS OF (+/-)-3,4-DI-O-ACETYL-1,2,5,6-TETRA-O-BENZYL-MYO-INOSITO ON HEATING AND COOLING: A '

Racemic 1,2-O-isopropylidene-myo-inositol was converted into a mixture of 1,2:5,6-, 1,2:3,4-, and 1,2:4,5-di-O-isopropylidene-myo-inositols which were resolved by g.l.c.The 1,2:4,5 and 1,2:5,6- isomers were isolated from the mixture as benzoate derivative