129879-49-8

Upstream product

• 23393-20-6 (+/-)-3-O-benzyl-1,2:4,5-di-O,O-cyclohexylidene-myo-inositol 
• 106-95-6 allyl bromide 
• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 1670-47-9 1,1-diethoxycyclohexane 

Downstream Products

• 136282-32-1 6-O-allyl-3-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 136282-33-2 4-O-allyl-1,5,6-tri-O-benzyl-3-O-tert-butyldimethylsilyl-myo-inositol 
• 131146-91-3 (+/-)-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 

Relevant academic research and scientific papers

Synthesis of racemic 3-methylphosphonate analogues of myo-inositol 3,4-bis- and 1,3,4-trisphosphate

The partially benzyl protected myo-inositol derivatives 11a and 11b, the C-4 and C-1,4 hydroxyl function(s) of which are protected with temporary trans-prop-1-enyl protecting group(s), were readily converted into the respective title compounds 18a and 18b by sequential methylphosphonylation, mild cleavage of the trans-prop-1-enyl group(s), phosphorylation and removal of all permanent benzyl protecting groups.