187877-40-3

Upstream product

• 65-85-0 benzoic acid 
• 187877-05-0 (1S,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanol 
• 187876-91-1 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1-trimethylsilyloxy-1-cyclopentene 
• 187876-97-7 (3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanone 
• 141389-79-9 (3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclopentanone 

Downstream Products

• 187877-56-1 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1S-azido-2R-fluorocyclopentane 
• 187878-48-4 9-[(1S,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purine 
• 187878-57-5 9-[(1S,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-9H-purin-6-ylamine 
• 187877-16-3 (1R,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanol 

Relevant academic research and scientific papers

Synthesis of carbocyclic 2',3'-dideoxy-2'-fluoro-3'-C-hydroxymethyl nucleoside analogues as potential inhibitors of HIV and HSV

The synthesis of four isomerically pure fluoro-carbocyclic adenosine and guanosine analogues is described. The 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-2-fluoropentan- 1-ol derivatives 22, 23, 24 and 25 synthesised from enantiomerically pure 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-cyclopentanone (18), were coupled with chloropurines using the Mitsunobu procedure to give 10, 11, 12, 14 and 16 or converted to their corresponding 1-amino derivatives, from which the fluoro-carbocyclic guanosine analogues 13, 15 and 17 were prepared. Compounds 10-17 were evaluated as potential anti-viral agents but were found to be inactive.