128442-41-1

Upstream product

• 98-88-4 benzoyl chloride 
• 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 
• 140195-49-9 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(trifluoromethylsulfonyl)-chiro-inositol 
• 134109-17-4 D-3-O-benzoyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 134073-32-8 2L-(2,3,5/4,6)-2,3:4,5-di-O-cyclohexylidene-6-O-methyl-2,3,4,5,6-pentahydroxycyclohexanone 
• 134109-12-9 D-1,2:5,6-di-O-cyclohexylidene-4-O-methyl-myo-inositol 
• 60504-85-0 D-3-O-benzoyl-1,2:5,6-di-O-cyclohexylidene-4-O-methyl-myo-inositol 
• 131432-86-5 D-3-O-benzoyl-1,2-O-cyclohexylidene-myo-inositol 
• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 801301-08-6 D-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-cyclohexylidene-myo-inositol 
• 55123-25-6 D-1,2-O-cyclohexylidene-myo-inositol 
• 39681-62-4 D-1,2-O-cyclohexylidene-3,4,5,6-tetra-O-benzoyl-myo-inositol 

Downstream Products

• 128352-26-1 D-3,4,5,6-tetra-O-benzoyl-1-O-triethylsilyl-myo-inositol 
• 134932-19-7 (+)-1D-1,2,4,5,6-O-pentabenzoyl-myo-inositol 
• 134865-98-8 D-1,3,4,5,6-penta-O-benzoyl-1-O-triethylsilyl-myo-inositol 
• 128352-27-2 D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol 
• 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 
• 134865-99-9 C₄₁H₃₃O₁₄P 
• 128441-63-4 D-(+)-myo-inositol 1-phosphate bis(cyclohexylammonium) salt 
• 138258-57-8 1D-(1,3/2,4)-1,2,3,4-tetra-O-benzoyl-5-cyclohexene-1,2,3,4-tetrol 
• 138223-79-7 D-3,4,5,6-tetra-O-benzoyl-1,2-O-thiocarbonyl-myo-inositol 

Relevant academic research and scientific papers

Resolution of synthetically useful myo-inositol derivatives using the chiral auxiliary O-acetylmandelic acid

Efficient methods for the resolution of various myo-inositol derivatives have been developed using O-acetylmandelic acid (OAM) as the chiral auxiliary. Various methods of introduction of the chiral auxiliary have been compared. DCC mediated coupling betwe

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.

A Chiral Synthesis of D-myo-Inositol 1-Phosphate Starting from L-Quebrachitol

A naturally occurring optically active cyclitol, L-quebrachitol (1L-2-O-methyl-chiro-inositol), was stereoselectively transformed into myo-inositol derivatives via an oxidation-reduction process.The methyl ether was cleaved chemoselectively with AlCl3NaI

Chiral synthesis of D-Myo-inositol 1-phosphate starting from L-querbrachitol

D-Myo-inositol 1-phosphate was synthesized from L-quebrachitol via stereoselective inversion of a 3-hydroxyl group and chemoselective demethylation.

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