418766-97-9

Upstream product

• 418766-81-1 [2-hydroxy-3-(6-amino-9H-purin-9-yl)propyl] 2-O-benzyl-3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 
• 418766-94-6 [(2S)-2-hydroxy-3-(6-amino-9H-purin-9-yl)propyl] 3,4-di-O-benzoyl-2-O-benzyl-α-D-xylopyranoside 
• 100-39-0 benzyl bromide 
• 66224-66-6 adenine 
• 201043-07-4 allyl 3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 
• 196859-39-9 allyl 3,4-di-O-benzoyl-2-O-benzyl-α-D-xylopyranoside 
• 418766-93-5 [(2R)-2,3-epoxypropyl] 3,4-di-O-benzoyl-2-O-benzyl-α-D-xylopyranoside 

Downstream Products

• 418767-00-7 9-[3-[3-benzyloxy-4,5-bis-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxy)-tetrahydro-pyran-2-yloxy]-2-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxy)-propyl]-9H-purin-6-ylamine 

Relevant academic research and scientific papers

D-myo-Inositol-1,4,5-trisphosphate and adenophostin mimics: Importance of the spatial orientation of a phosphate group on the biological activity

Three different routes for the synthesis of heterocyclic analogues of the second messenger D-myo-inositol-1,4,5-trisphosphate (InsP3) and the natural adenophostins, starting from allyl D-xyloside are described. The two diastereoisomers at C-2 o