404893-41-0

Upstream product

• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 106221-09-4 (S)-1-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-prop-2-en-1-ol 

Downstream Products

• 404893-44-3 Octadecanoic acid (R)-3-{benzyloxy-[(1S,2R,3S,4S,5R,6R)-2,4-bis-benzyloxy-6-benzyloxymethoxy-3,5-bis-(4-methoxy-benzyloxy)-cyclohexyloxy]-phosphoryloxy}-2-butyryloxy-propyl ester 
• 404893-46-5 Octadecanoic acid (R)-3-[benzyloxy-((1S,2R,3S,4S,5R,6R)-2,4-bis-benzyloxy-6-benzyloxymethoxy-3,5-dihydroxy-cyclohexyloxy)-phosphoryloxy]-2-butyryloxy-propyl ester 
• 404893-42-1 Benzoic acid (1S,2R,3S,4S,5R,6R)-2,4-bis-benzyloxy-6-benzyloxymethoxy-3,5-bis-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 404893-43-2 (1S,2S,3R,4S,5R,6S)-2,4-Bis-benzyloxy-6-benzyloxymethoxy-3,5-bis-(4-methoxy-benzyloxy)-cyclohexanol 
• 404893-38-5 Benzoic acid (1R,2R,3S,4R,5S,6R)-2,4-bis-benzyloxy-6-hydroxy-3,5-bis-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 404893-37-4 (3S,4R,5R,6S)-3,5-Bis-benzyloxy-4,6-bis-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 404893-36-3 C₃₆H₃₈O₆ 
• 404893-35-2 (1R,2R,3S,6S)-2,6-Bis-benzyloxy-cyclohex-4-ene-1,3-diol 

Relevant academic research and scientific papers

Synthesis of L-α-phosphatidyl-D-myo-inositol 3,5-bisphosphate from D-glucose

Efficient synthesis of L-α-phosphatidyl-D-myo-inositol 3,5-bisphosphate was achieved from 1,2,5,6-diisopropylidene-D-glucose by utilizing ring-closing metathesis and catalytic OsO4 dihydroxylation.

Intra-molecular nitrone-olefin cycloaddition of d-glucose derived allylic alcohol: synthesis of new aminocyclohexitols

Diastereo- and regioselelective intra-molecular nitrone-olefin cycloaddition reaction of in situ generated N-benzylnitrones, obtained from d-glucose derived precursors 5a/5b furnished dihydroxy functionalized isoxazolidines. The N-O bond reductive cleavag