608880-27-9

Upstream product

• 15205-57-9 tribenzyl phosphite 
• 608880-22-4 5-dibenzyl D-1,2-O-cyclohexylidene-6-O-levulinoyl-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol phosphate 
• 608880-24-6 5-dibenzyl D-1,2-O-cyclohexylidene-6-O-levulinoyl-myo-inositol phosphate 
• 678142-80-8 D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol 
• 171336-58-6 1D-1,2-O-cyclohexylidene-6-O-(4-oxopentanoyl)-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol 
• 171336-57-5 1D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol 
• 123-76-2 levulinic acid 
• 608880-26-8 C₄₅H₅₂O₁₄P₂ 

Downstream Products

• 608880-28-0 Hexadecanoic acid (R)-2-{benzyloxy-[(1R,2R,3R,4R,5S,6R)-3,5-bis-(bis-benzyloxy-phosphoryloxy)-2,4-dihydroxy-6-(4-oxo-pentanoyloxy)-cyclohexyloxy]-phosphoryloxy}-1-hexadecanoyloxymethyl-ethyl ester 

Relevant academic research and scientific papers

Chemical Resolution of 1,2-O-Cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol and Synthesis of Phosphatidyl-D-myo-inositol 3,5-Bisphosphate from Both L- and D-Enantiomers

Chemical resolution of a versatile starting material, 1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol, which is used to access naturally occurring inositol phosphates and phosphatidylinositol phosphates, is described. Starting

Enantiomerically Convergent Synthesis of Phosphatidyl-D-myo-inositol 3,5-Bisphosphate from Both L- And D-1,2-O-Cyclohexylidene-myo-inositol

The synthesis of phosphatidyl-D-myo-inositol 3,5-bisphosphate [PtdIns(3,5)P2] has been conveniently accomplished via convergent routes starting from both enantiomers, 1,2-O-cyclohexylidene-myo-inositol. The synthetic strategy involves completely regiosele