114342-75-5

Upstream product

• 990-91-0 dibenzyl [[bis(benzyloxy)phosphoryl]oxy]phosphonate 
• 35949-66-7 (+/-)-1,4-di-O-benzyl-2,3-O-cyclohexylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 1122-84-5 1-ethoxycyclohexene 
• 6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol 
• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 23486-92-2 3,6-di-O-benzyl-1,2:4,5-di-O-cyclohexylidene-D(L)-myo-inositol 
• 100-44-7 benzyl chloride 

Downstream Products

• 114419-02-2 (+)-3,6-di-O-benzyl-4,5-bis-O-(di-O-benzylphospho)-myo-inositol 
• 114342-69-7 L-3,6-di-O-benzyl-4,5-di-O-(dibenzyl phosphoryl)-myo-inositol 
• 120065-90-9 Phosphoric acid dibenzyl ester (1R,2S,3S,4R,5S,6R)-2,5-bis-benzyloxy-4,6-bis-(bis-benzyloxy-phosphoryloxy)-3-triethylsilanyloxy-cyclohexyl ester 
• 120065-86-3 Benzoic acid (1R,2S,3R,4R,5S,6S)-2,5-bis-benzyloxy-3,4-bis-(bis-benzyloxy-phosphoryloxy)-6-triethylsilanyloxy-cyclohexyl ester 
• 120065-89-6 Phosphoric acid dibenzyl ester (1R,2R,4S,5S,6R)-2,5-bis-benzyloxy-6-(bis-benzyloxy-phosphoryloxy)-3-oxo-4-triethylsilanyloxy-cyclohexyl ester 
• 120065-87-4 Benzoic acid (1S,2S,3R,4R,5S,6S)-2,5-bis-benzyloxy-3,4-bis-(bis-benzyloxy-phosphoryloxy)-6-hydroxy-cyclohexyl ester 
• 141724-55-2 Phosphoric acid dibenzyl ester (1S,2R,3S,4S,5R,6S)-2,5-bis-benzyloxy-6-(bis-benzyloxy-phosphoryloxy)-3-hydroxy-4-triethylsilanyloxy-cyclohexyl ester 
• 141725-53-3 Phosphoric acid dibenzyl ester (1R,2S,3R,4R,5S,6R)-2,5-bis-benzyloxy-6-(bis-benzyloxy-phosphoryloxy)-3-hydroxy-4-triethylsilanyloxy-cyclohexyl ester 

Relevant academic research and scientific papers

Synthesis and Some Properties of D-myo-Inositol 1,4,5-Tris(dihydrogen phosphate)

Optically active myo-inositol 1,4,5-tris(dihydrogen phosphate) 1, which has now been recognized as a second messenger in a new intracellular signal transduction system, has been prepared starting from myo-inositol.The key step, phosphorylation of an adequately protected polyhydroxy derivative, was accomplished by three methods, among which a phosphoramidite method using a new phosphitylating agent, o-xylylene N,N-diethylphosphoramidite, gave the triphosphoric ester in quantitative yield.Optical resolution was effectively realized by derivatization into diastereoisomeric l-menthoxyacetic esters.NMR spectra and optical rotation are shown to depend on the pH of an aqueous solution of compound 1.

Synthesis and biological properties of 2-substituted myo-inositol 1,4,5-trisphosphate analogues directed toward affinity chromatography and photoaffinity labeling

A series of myo-inositol 1,4,5-trisphosphate analogues with the 2-acyl substituents p-aminobenzoyl (7), p-azidobenzoyl (8), 4--2-hydroxyphenylazo>benzoyl (9), and cis,trans-4-aminocyclohexylcarbonyl (10) were synthesised and examine

A VERSATILE INTERMEDIATE, D-4,5-BIS(DIBENZYL PHOSPHORYL)-MYO-INOSITOL DERIVATIVE FOR SYNTHESIS OF INOSITOL PHOSPHATES. SYNTHESIS OF 1,2-CYCLIC-4,5-, 1,4,5-, AND 2,4,5-TRISPHOSPHATE

Practical synthesis of D-myo-inositol 1,2-cyclic-4,5-, 1,4,5-, and 2,4,5-trisphosphate was accomplished from the key synthetic intermediate, D-3,6-di-O-benzyl-4,5-di-O-(dibenzyl phosphoryl)-myo-inositol.