134932-19-7

Upstream product

• 551-72-4 inositol 
• 98-88-4 benzoyl chloride 
• 131432-86-5 D-3-O-benzoyl-1,2-O-cyclohexylidene-myo-inositol 
• 73763-43-6 D-1,2,4,5,6-penta-O-benzoyl-3-O-formyl-chiro-inositol 
• 99044-47-0 1,2,3,4,5-penta-O-benzoyl-6-O-benzyl-myo-inositol 
• 18391-42-9 D-1,2,4,5,6-penta-O-benzoyl-3-O-methyl-chiro-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 
• 128442-41-1 D-3,4,5,6-tetra-O-benzoyl-myo-inositol 
• 153265-90-8 (-)-1D-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol 
• 153325-42-9 4,6-di-O-benzoyl-myo-inositol 
• 98510-20-4 myo-Inositol orthoformate 
• 134865-98-8 D-1,3,4,5,6-penta-O-benzoyl-1-O-triethylsilyl-myo-inositol 

Downstream Products

• 128352-27-2 D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol 
• 128441-63-4 D-(+)-myo-inositol 1-phosphate bis(cyclohexylammonium) salt 
• 134865-99-9 C₄₁H₃₃O₁₄P 

Relevant academic research and scientific papers

Enzyme Assisted Synthesis of Enantiomerically Pure myo-Inositol Derivatives - Chiral Building Blocks for Inositol Polyphosphates

Using a short and facile synthetic protocol involving highly selective, regio- and enentioselective enzymatic esterifications as key reaction steps, readily available myo-inositol is converted into optically pure 1D-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol (-) - 5, a selectively protected central intermediate for the preparation of numerous inositol phosphates.

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 1D- AND 1L-4-O-BENZYL-myo-INOSITOL, 1D-4-O-α-L-FUCOPYRANOSYL-myo-INOSITOL (IDENTICAL TO A NATURAL GLYCOSIDE), AND 1L-4-O-α-L-FUCOPYRANOSYL-myo-INOSITOL

The α-L-fucopyranosyl-myo-inositol isolated from human urine has been proved to be the 1D-4-O-myo-inositol derivative by unambiguous syntheses of this substance and of the diastereomeric 1L-4-O-myo-inositol derivative.The chiral penta-O-benzoyl-myo-inosit