124990-69-8

Upstream product

• 124901-27-5 C₅₈H₆₄N₄O₁₇P₂ 
• 71788-34-6 1⁽³⁾,4⁽⁶⁾-di-O-benzyl-5,6⁽⁴⁾-di-O-(dianilido)phospho-sn-myo-inositol 
• 127833-07-2 C₄₇H₅₀N₄O₈P₂ 
• 98906-25-3 (±)-1,2-O-isopropylidene-3,6-di-O-benzyl-myo-inositol 
• 5625-99-0 N,N'-diphenylphosphorodiamidic chloride 

Downstream Products

• 124989-66-8 1⁽³⁾,6⁽⁴⁾-di-O-benzyl-4⁽⁶⁾,5-bis-O-(dianilinophosphinyl)-sn-myo-inositol 
• 77533-51-8 1⁽³⁾,4⁽⁶⁾,5-tris-O-(dianilidophospho)-3⁽¹⁾,6⁽⁴⁾-di-O-benzyl-sn-myo-inositol 
• 120710-76-1 cyclohexylammonium salt of sn-myoinositol 1⁽³⁾,4⁽⁶⁾,5-triphosphate 
• 124901-27-5 C₅₈H₆₄N₄O₁₇P₂ 
• 124901-27-5 C₅₈H₆₄N₄O₁₇P₂ 

Relevant academic research and scientific papers

INVESTIGATIONS IN THE FIELD OF DERIVATIVES OF ASYMMETRICALLY SUBSTITUTED myo-INOSITOL. XXXVI. SEPARATION OF DIASTEREOMERIC CARBOHYDRATE DERIVATIVES OF myo-INOSITOL BY THE HPLC METHOD

The possibility has been shown of using the HPLC method for separating diastereomeric compounds of myo-inositol obtained under the conditions of the transesterification of racemic myo-inositol derivatives with D-mannose (ethyl orthoacetate).The optically active myo-inositol derivatives obtained can be used for the synthesis of myo-inositol phosphates with various structures.

TOTAL SYNTHESES OF CHIRAL sn-myo-INOSITOL-1,4,5-TRISPHOSPHATE AND ITS ENANTIOMER.

sn-myo-Inositol-1,4,5-trisphosphate (Ins(1,4,5)P3) and its enantiomers are prepared by synthesis of suitably protected myo-inositols, separation of enantiomers via the formation of D-mannose diastereomeric derivatives and selective phosphorylations.