132405-98-2

Upstream product

• 132360-43-1 3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-6-O-para-methoxybenzyl-D(L)-myo-inositol 
• 100-39-0 benzyl bromide 
• 13035-66-0 L-3,4-di-O-benzyl-1,2-O-cyclohexylidene-chiro-inositol 
• 23393-20-6 (+/-)-3-O-benzyl-1,2:4,5-di-O,O-cyclohexylidene-myo-inositol 
• 132360-44-2 3-O-benzyl-1,2-O-cyclohexylidene-6-O-para-methoxybenzyl-D(L)-myo-inositol 
• 132360-45-3 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-para-methoxybenzyl-D(L)-myo-inositol 

Downstream Products

• 133076-47-8 C₄₅H₅₈O₈ 
• 133076-47-8 C₄₅H₅₈O₈ 
• 132360-48-6 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-(2'-O-benzoyl-3',4',6'-tri-O-benzyl-α-D-mannopyranosyl)-D(L)-myo-inositol 
• 54422-83-2 6-O-(α-D-mannopyranosyl)-D-myo-inositol 
• 132360-49-7 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-(3',4',6'-tri-O-benzyl-α-D-mannopyranosyl)-L-myo-inositol 
• 132437-47-9 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-(3',4',6'-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 132360-51-1 3,4,5-tri-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 132360-51-1 3,4,5-tri-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-L-myo-inositol 
• 132360-52-2 1-O-allyl-3,4,5-tri-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-L-myo-inositol 
• 132360-52-2 1-O-allyl-3,4,5-tri-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 132360-50-0 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-L-myo-inositol 
• 132360-50-0 3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 124684-95-3 1-O-allyl-2,3,4,5-tetra-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-L-myo-inositol 
• 124684-95-3 1-O-allyl-2,3,4,5-tetra-O-benzyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 

Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF PARTIALLY PROTECTED 2-AZIDO-2-DEOXY-D-GLUCOSYL D-MYO-INOSITOL: PRECURSOR OF A POTENTIAL INSULIN MIMETIC AND MEMBRANE PROTEIN ANCHORING SITE

Racemic and partially protected myo-inositol derivative 5 was coupled stereospecifically with the 2-azido-2-deoxy-glucosyl trichloroacetimidate donor 8.Optical resolution of the thus obtained diastereoisomeric mixture of dimers by silica gel column chromatography, and further protective group manipulations, afforded the suitably protected title compound 14.

THE PREPARATION OF CYCLOHEXANEPENTOLS FROM INOSITOLS BY DEOXYGENATION

Several cyclohexapenetols heva been synthesized from inositols by blocking all but one hydroxyl group, converting the free hydroxyl group into its S-methyl dithiocarbonate, and treating it with tributylstannane.Suitable blocking-groups are methyl, benzyl, and methylthiomethyl ethers, and acetals.One cyclohexanepentol was prepared by the reductive deamination of an aminodeoxyinositol.