1054657-08-7

Upstream product

• 214332-45-3 Acetic acid (1S,2R,3R,4S,5S,6R)-3,4-bis-benzyloxy-2,6-dihydroxy-5-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 214068-17-4 methyl 2-O-(p-methoxybenzyl)-6-O-trityl-α-D-glucopyranoside 
• 214068-28-7 methyl (Z)-3,4-O-dibenzyl-2-O-(p-methoxybenzyl)-6-O-acetyl-α-D-glucos-5-enopyranoside 
• 214068-33-4 Acetic acid (1R,3S,4R,5S,6R)-3,4-bis-benzyloxy-6-hydroxy-5-(4-methoxy-benzyloxy)-2-oxo-cyclohexyl ester 
• 214068-24-3 methyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-α-D-glucopyranoside 
• 1054640-17-3 (2S,3S,4S,5R,6S)-3,4-Bis-benzyloxy-6-methoxy-5-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-carbaldehyde 
• 214068-00-5 methyl 2-O-(p-methoxybenzyl)-4,6-O-(p-methoxybenzylidene)-α-D-glucopyranoside 
• 214068-12-9 methyl 2-O-(p-methoxybenzyl)-α-D-glucopyranoside 
• 14347-78-5 1,2-O-isopropylidene-D-glycerol 
• 108549-21-9 benzyl-N,N,N',N'-tetraisopropylphosphorodiamidite 
• 100-39-0 benzyl bromide 
• 3587-60-8 Benzyloxymethyl chloride 
• 214068-63-0 Diisopropyl-phosphoramidous acid benzyl ester (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 214068-39-0 (1S,2S,3S,4S,5R,6S)-3,4-Bis-benzyloxy-2,6-bis-benzyloxymethoxy-5-(4-methoxy-benzyloxy)-cyclohexanol 

Downstream Products

• 1054640-00-4 Phosphoric acid benzyl ester (1S,2R,3S,4S,5R,6R)-3,4-bis-benzyloxy-2,6-bis-benzyloxymethoxy-5-(bis-benzyloxy-phosphoryloxy)-cyclohexyl ester (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 1053738-99-0 Phosphoric acid benzyl ester (1R,2R,3S,4R,5R,6R)-3,4-bis-benzyloxy-2,6-bis-benzyloxymethoxy-5-hydroxy-cyclohexyl ester (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 

Relevant academic research and scientific papers

Asymmetric Total Synthesis of Phosphatidylinositol 3-Phosphate and 4-Phosphate Derivatives

New asymmetric syntheses of phosphatidylinositol 3-phosphate (PtdIns(3)P) and phosphatidylinositol 4-phosphate (PtdIns(4)P) derivatives are described. Key intermediates were used to prepare diacylglyceryl moieties with dibutyryl, dioctanoyl, and dihexadecanoyl chains. In addition, a modified route provided PtdIns(3)P and PtdIns(4)P triesters with P-1-linked aminopropyl groups for preparation of affinity probes. The synthesis of the inosityl precursor employed a dibutyltin oxide-mediated p-methoxybenzyl (PMB) etherification to give either the 2-PMB- or the 3-PMB-protected glucopyranosides. The Ferrier rearrangement was used to convert suitably protected glucose derivatives to enantiomerically pure, differentially protected D-myo-inositol key intermediates. A versatile phosphoramidite reagent was employed to allow synthesis of PtdInsPn derivatives with diacylglyceryl moieties of different chain lengths.