127753-47-3

Upstream product

• 64767-30-2 3-endo-benzyloxytricyclo<3.2.0.0^2,7>heptan-6-one 

Downstream Products

• 127753-50-8 6endo-benzyloxy-8syn-fluoro-3-oxabicyclo<3.2.1>octan-2-one 
• 135387-36-9 <(1β,2β,3β,4β)-4-benzyloxy-2-fluoro-3-(hydroxymethylcyclopentyl)>amide 
• 135387-37-0 <(1β,2β,3β,4β)-4-benzyloxy-3-(tert-butyldiphenylsilyloxymethyl)-2-(fluorocyclopentyl)>amine 
• 135387-47-2 <(1β,2β,3β,4β)-4-benzyloxy-3-(tert-butyldiphenylsilyloxymethyl)-2-(fluorocyclopentyl)>amide 
• 127753-51-9 1-<(1β,2β,3β,4β)-4-benzyloxy-3-(tert-butyldiphenylsilyloxymethyl)-2-fluorocyclopentyl>-5-methylpyrimidine-2,4(1H,3H)-dione 
• 135387-38-1 3-methoxy-2-methyl-N-<(1β,2β,3β,4β)-4-benzyloxy-3-(tert-butyldiphenylsilyloxymethyl)-2-fluorocyclopentylaminocarbonyl>prop-2-enamide 

Relevant academic research and scientific papers

The Potential for Using Carbocyclic Nucleosides for the Treatment of AIDS. Part 1. Preparation of Some Analogues for Azidothymidine (AZT)

The tricyclic compound 10 was converted into the fluoronorbornane 11 and the norbornanol 23 using fluoride ion and water respectively.The fluoro compound 11 was converted into the carbocyclic nucleosides 5 and 7 by a series of stereocontrolled reactions.S