134039-19-3

Upstream product

• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 129879-48-7 (+/-)-1,2:4,5-di-O-cyclohexylidene-3-O-allyl-myo-inositol 
• 134039-17-1 C₂₃H₃₂O₇ 
• 134039-16-0 C₂₉H₄₀O₇ 
• 134039-18-2 C₃₇H₄₄O₇ 

Downstream Products

• 134039-20-6 1-((1R,2S,3R,4R,5R,6R)-4-Allyloxy-2,3,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene 
• 26277-05-4 1,2,4,5,6-penta-O-benzyl-sn-myo-inositol 
• 114218-29-0 1L-1-O-allyl-2,3,4,5,6-penta-O-benzyl-myo-inositol 
• 134039-23-9 Methyl-phosphonic acid benzyl ester (1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 134039-25-1 ((S)-3,4-Dihydroxy-butyl)-phosphonic acid benzyl ester (1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 134039-24-0 [2-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-ethyl]-phosphonic acid benzyl ester (1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 134039-27-3 Hexadecanoic acid (S)-3-[benzyloxy-((1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-hydroxy-cyclohexyloxy)-phosphoryl]-1-hexadecanoyloxymethyl-propyl ester 
• 134039-26-2 Hexadecanoic acid (S)-3-{benzyloxy-[(1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyloxy]-phosphoryl}-1-hexadecanoyloxymethyl-propyl ester 
• 134039-22-8 (1R,4S)-4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (1S,2R,3R,4S,5S,6R)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 134039-22-8 (1R,4S)-4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (1S,2S,3R,4S,5S,6S)-2,3,5,6-tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexyl ester 
• 134039-21-7 (1R,2R,3S,4R,5R,6R)-2,3,5,6-Tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexanol 
• 134039-21-7 (1R,2S,3S,4R,5R,6S)-2,3,5,6-Tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexanol 
• 134039-21-7 (1R,2R,3S,4R,5R,6R)-2,3,5,6-Tetrakis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohexanol 
• 134039-20-6 1-((1R,2S,3R,4R,5R,6R)-4-Allyloxy-2,3,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene 

Relevant academic research and scientific papers

Synthesis of phosphonate analogues of myo-inositol phospholipids

The phosphonate analogues I and II of Ptdlns and Ptdlns[4]P, respectively, were prepared by alkylation of the α-lithio anion of a properly protected D-myo-inositol methylphosphonate diester with 1,2-isopropylidene-sn-glycerol 3-trifluoromethanesulfonate, followed by protective group manipulation and deprotection.