864372-79-2

Upstream product

• 112212-81-4 (+/-)-(1S,2R,3R,4S)-1,4-diacetoxy-2,3-dibromocyclohex-5-ene 
• 169529-92-4 (+)-(1R,2S,3S,4R)-2,3-dibromocyclohex-5-ene-1,4-diol 
• 1623-08-1 phosphoric acid dibenzyl ester 
• 222420-77-1 (1S,2R,3R,4S)-1,4-bis-O-(di-O-benzylphospho)conduritol B 
• 281206-67-5 (1S,2R,3R,4S)-2,3-di-O-acetyl-1,4-bis-O-(di-O-benzylphospho)conduritol B 

Downstream Products

• 864372-95-2 2,4,5-tris-O-acetyl-3,6-bis-O-(di-O-benzylphospho)-D-myo-inositol 
• 864372-80-5 4,5-di-O-acetyl-3,6-bis-O-(di-O-benzylphospho)-1,2-bis-O-(3-oxo-1,5-dihydro-3λ⁵-2,4,3-benzodioxaphosphepin-3-yl)-D-myo-inositol 
• 864372-96-3 Acetic acid (1R,2R,3S,4S,5R,6R)-3,4-diacetoxy-2,5-bis-(bis-benzyloxy-phosphoryloxy)-6-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxy)-cyclohexyl ester 

Relevant academic research and scientific papers

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (part 1): Via symmetrical conduritol B derivatives

A practical route is described for the preparation of myo-inositol polyphosphates. Optically pure myo-inositol derivatives can be prepared from p-benzoquinone in both forms by enzymatic resolution of a C2- symmetric diacetoxyconduritol B key in

De novo synthesis of the enantiomers Ins(1,2,3,4)P4 and Ins(1,2,3,6)P4-regiospecificity of their enzymatic dephosphorylation

The first total synthesis of Ins(1,2,3,4)P4 and Ins(1,2,3,6)P4 is presented. Starting from p-benzoquinone, we took advantage of the C2-symmetry of conduritol-B intermediates. The target compounds were dephosphorylated by s