796883-88-0

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 376590-85-1 1-O-diphenylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol 

Downstream Products

• 796883-89-1 3,5-O-bis(t-butyldimethylsilyl)-1-O-dibenzylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol 
• 796883-90-4 Octanoic acid (S)-2-{benzyloxy-[(1R,2S,3S,4R,5R,6S)-2,4,6-tris-benzyloxy-3-(bis-benzyloxy-phosphoryloxy)-5-hydroxy-cyclohexyloxy]-phosphoryloxy}-1-octanoyloxymethyl-ethyl ester 
• 797038-12-1 1-O-dibenzylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol 

Relevant academic research and scientific papers

Catalyst-dependent syntheses of phosphatidylinositol-5-phosphate-DiC8 and its enantiomer

Peptide-based catalysts have been applied to the enantioselective syntheses of the title compounds, with this being the first report of the synthesis of an ent-PI5P analogue. The key steps in the synthesis involve asymmetric phosphorylation catalysis. Add

Streamlined synthesis of phosphatidylinositol (PI), PI3P, PI3, 5P 2, and deoxygenated analogues as potential biological probes

Highly direct total syntheses of phosphatidylinositol (PI), phosphatidylinositol-3-phosphate (PI3P), phosphatidylinositol-3,5-bisphosphate (PI3,5P2), and a range of deoxygenated versions are reported. Each synthesis is carried out to deliver th

Asymmetric syntheses of phosphatidylinositol-3-phosphates with saturated and unsaturated side chains through catalytic asymmetric phosphorylation

Highly direct asymmetric syntheses of phosphatidylinositol-3-phosphate (PI3P) in each enantiomerically pure form have been achieved. The key step involves catalytic asymmetric phosphorylation of meso-myo-inositol derivatives through desymmetrization. Prot