130792-11-9

Upstream product

• 129662-36-8 (1R,2S,3S,4R,5R,6S)-3,6-Bis-benzyloxy-4,5-bis-(2-methoxy-ethoxymethoxy)-cyclohexane-1,2-diol 
• 129662-35-7 C₂₈H₃₈O₈ 
• 100-39-0 benzyl bromide 
• 130659-80-2 (4S,5R,6S)-4-Hydroxy-5,6-bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-enone 
• 129662-34-6 (1S,4S,5R,6R)-5,6-Bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-ene-1,4-diol 
• 130659-82-4 (5S,6S)-5,6-Bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-ene-1,4-dione 
• 129662-35-7 (+/-)-1,2,4/3-1,4-Di-O-benzyl-2,3-O-(2-methoxyethoxymethyl)cyclohex-5-ene-1,2,3,4-tetrol 
• 129662-33-5 trans-5,6-Di-(2-methoxyethoxymethyl)-2,3-dioxabicyclo<2.2.2>oct-7-ene 
• 129662-34-6 (+/-)-1,2,4/3-2,3-Di-O-(2-methoxyethoxymethyl)cyclohex-5-ene-1,2,3,4-tetrol 
• 129662-32-4 trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol 
• 17793-95-2 (1RS,2RS)-cyclohexa-3,5-diene-1,2-diol 
• 129662-36-8 (+/-)-1,4-Di-O-benzyl-2,3-di-O-(2-methoxyethoxymethyl)-chiro-inositol 
• 3970-21-6 2-Methoxyethoxymethyl chloride 

Downstream Products

• 129662-38-0 C₃₉H₅₄O₁₂ 
• 98906-30-0 (±)-2,3,6-tri-O-benzyl-myo-inositol 
• 114342-70-0 Phosphoric acid dibenzyl ester (1R,2R,3S,4R,5R,6S)-2,3,6-tris-benzyloxy-4,5-bis-(bis-benzyloxy-phosphoryloxy)-cyclohexyl ester 
• 129662-38-0 C₃₉H₅₄O₁₂ 
• 115184-71-9 (+/-)-1,3,4-tri-O-benzyl-myo-inositol 
• 114342-70-0 (+/-)-nona-O-benzyl-2,4,5-myo-inositol trisphosphate 

Relevant academic research and scientific papers

Synthesis of racemic 6-deoxy-6-fluoro-chiro-inositol 2,3,5-trisphosphate

The synthesis of (±)-6-deoxy-6-fluoro-chiro-inositol 2,3,5-trisphosphate (4) is reported, starting from cyclohexa-1,4-diene. A key step involved the stereospecific 1,4-addition of singlet oxygen to trans-1,2-di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene

Total synthesis of myo-inositol polyphosphates from benzene via conduritol B derivatives

The four (±)-myo-inositol phosphates 1,4,5-IP3 (1), 2,4,5-IP3 (15), 1,2,4,5-IP4 (17) and 4,5-IP2 (19) have been synthesised from benzene, using the protected conduritol B (10) as the key intermediate.

TOTAL SYNTHESIS OF chiro-INOSITOL 2,3,5-TRISPHOSPHATE: A myo-INOSITOL 1,4,5-TRISPHOSPHATE ANALOGUE FROM BENZENE VIA PHOTO-OXIDATION

The inositol tris- and tetrakis-phosphate analogues (4) and (14) have been synthesized from benzene by a sequence including reaction of singlet oxygen with a trans-cyclohexa-3,5-diene-1,2-diol (3) derivative.