81562-14-3

Upstream product

• 23486-92-2 3,6-di-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 13035-66-0 L-3,4-di-O-benzyl-1,2-O-cyclohexylidene-chiro-inositol 
• 100-44-7 benzyl chloride 
• 58526-04-8 1D-1,4-di-O-benzyl-2,3-O-cyclohexylidene-myo-inositol 
• 34361-60-9 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol 

Downstream Products

• 81562-16-5 D-1,2,5-tri-O-benzyl-3,4-O-cyclohexylidene-1,3,4/2,5-cyclohexanepentol 
• 131473-37-5 1,4,6-tri-O-benzyl-2,3-O-cyclohexylidene-5-deoxy-5-fluoro-myo-inositol 
• 127982-77-8 (2,6/3,4,5)-2,3,6-tri-O-benzyl-4,5-O-cyclohexylidenepentahydroxycyclohexanone 

Relevant academic research and scientific papers

Substrate specificity of 2-deoxy-scyllo-inosose synthase, the starter enzyme for 2-deoxystreptamine biosynthesis, toward deoxyglucose-6-phosphates and proposed mechanism.

A crucial enzyme in the biosynthesis of the 2-deoxystreptamine aglycon of clinically important aminocyclitol antibiotics is 2-deoxy-scyllo-inosose synthase (DOIS), which is responsible for the initial carbocycle formation of 2-deoxy-scyllo-inosose (1) fro

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.