143060-89-3

Upstream product

• 100-39-0 benzyl bromide 
• 139744-48-2 trans-3,3-diethoxy-1,2-bis<(benzyloxy)methyl>cyclobutane 
• 126261-70-9 (+/-)-trans-1,2-bis-(3,3-diethoxycyclobutylen)methanol 
• 132164-72-8 trans-2,3-bis<(benzyloxy)methyl>cyclobutanone 

Downstream Products

• 142434-69-3 (+)-(1S,2S,3S)-2,3-bis<(benzyloxy)methyl>-1-cyclobutanol 
• 142343-78-0 (+)-(1R,2S,3S)-2-amino-7-<2,3-bis<(benzyloxy)methyl>cyclobutyl>pyrrolo<2,3-d>-pyrimidin-4(3H)-one 
• 142343-77-9 (+)-(1R,2S,3S)-2-amino-7-<2,3-bis<(benzyloxy)methyl>cyclobutyl>-4-chloropyrrolo<2,3-d>-pyrimidine 
• 142343-74-6 (+)-(1S,2S,3S)-2,3-bis<(benzyloxy)methyl>-1-cyclobutyl tosylate 
• 142343-75-7 C₂₀H₂₃N₃O₂ 
• 142343-76-8 (+)-(1R,2S,3S)-2,3-bis<(benzyloxy)methyl>cyclobutylamine 
• 142343-72-4 (+)-(1S,2S,3S)-2,3-bis<(benzyloxy)methyl>-1-cyclobutyl acetate 
• 142343-73-5 (-)-(1R,2R,3R)-2,3-bis<(benzyloxy)methyl>-1-cyclobutanol 

Relevant academic research and scientific papers

CHEMOENZYMATIC SYNTHESIS OF (-)-CARBOCYCLIC 7-DEAZAOXETANOCIN G

The enantioselective synthesis of (-)-(1R,2S,3S)-2-amino-7-pyrrolopyrimidin-4(3H)-one (5) as the 7-deaza analogue of carbocyclic oxetanocin G is described in 13 steps from trans-3,3-diethoxy-1,2-bis(hydroxymethyl)c