187980-85-4

Upstream product

• 187980-81-0 1D-1,3,4-tri-O-allyl-2,6-di-O-benzyl-5-O-p-methoxybenzyl-myo-inositol 
• 187841-87-8 Acetic acid (1S,2R,3R,4R,5R,6S)-2,3,5-tris-allyloxy-4,6-bis-benzyloxy-cyclohexyl ester 
• 187841-88-9 (1S,2S,3R,4R,5S,6R)-2,3,5-Tris-allyloxy-4,6-bis-benzyloxy-cyclohexanol 
• 141040-46-2 (1R,2R,3S,4R,5S,6S)-3,4,6-Tris-allyloxy-5-benzyloxy-cyclohexane-1,2-diol 
• 100-39-0 benzyl bromide 
• 77-76-9 2,2-dimethoxy-propane 
• 187980-83-2 (1R,2R,3R,4R,5S,6S)-3,5-Bis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexane-1,2,4-triol 

Downstream Products

• 180794-90-5 (-)-2,6-di-O-benzyl-1-O-(p-methoxybenzyl)-myo-inositol 
• 142436-05-3 1D-2,6-di-O-benzyl-1,5-di-O-p-methoxybenzyl-myo-inositol 
• 187980-83-2 (1R,2R,3R,4R,5S,6S)-3,5-Bis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexane-1,2,4-triol 

Relevant academic research and scientific papers

The preparation of racemic and enantiomerically pure myo-inositol derivatives as intermediates for the synthesis of phosphatidylinositol 3-, 3,4-bis-, and 3,4,5-tris-phosphates and for the synthesis of analogues of 1D-myo-inositol 1,3,4,5-tetrakisphosphat

Details of the products obtained by the tin-mediated allylation and benzylation of 1,2-O-isopropylidene-myo-inositol, which were previously described in a preliminary communication, are provided here. Some of the products from these reactions, particularl