33800-48-5

Upstream product

• 39681-62-4 1,4,5,6-tetra-O-benzoyl-2,3-O-cyclohexylidene-myo-inositol 
• 33800-47-4 (+/-)-3,4,5,6-tetra-O-benzoyl-1,2-O-isopropylidene-myo-inositol 

Downstream Products

• 132760-98-6 2,4,5,6-tetra-O-benzoyl-1-O-benzyl-myo-inositol 
• 117655-16-0 1,4,5,6-tetra-O-benzoyl-3-O-benzyl-myo-inositol 
• 117655-16-0 1,4,5,6-tetra-O-benzoyl-2-O-benzyl-myo-inositol 

Relevant academic research and scientific papers

Practical synthesis of all inositol stereoisomers from myo-inositol

Synthesis of six inositol stereoisomers was successfully carried out via conduritol intermediates prepared from myo-inositol. Dihydroxylation and epoxidation followed by ring opening of the conduritol B, C and F derivatives gave epi-, allo-, muco-, neo-, DL-chiro- and scyllo-inositol. The cis- inositol derivative, which may not be prepared by this approach, was synthesized in 5 steps via 2-O-benzoyl-myo-inositol orthoformate as the key intermediate.

SYNTHESIS OF SOME BENZYL AND METHYL ETHERS OF myo-INOSITOL

The 1D and 1L forms of 1,2,4,5,6- and 1,2,3,4,5-penta-O-methyl-myo-inositol have been prepared from the corresponding chiral mono-O-benzyl derivatives.Convenient preparations are also described of achiral derivatives of 1-, 2-, 4-, and 5-O-benzyl-myo-inos