141389-79-9

Upstream product

• 246518-20-7 (3S,4S)-bis(hydroxymethyl)cyclopentanone ethylene glycol ketal 
• 36237-88-4 7,8-trans-1,4-Dioxaspiro<4.4>nonan-7,8-dicarbonsaeure-dimethylester 

Downstream Products

• 187876-91-1 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1-trimethylsilyloxy-1-cyclopentene 
• 187878-48-4 9-[(1S,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purine 
• 187877-82-3 9-[(1R,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purine 
• 187877-62-9 9-[(1S,2S,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purine 
• 187878-12-2 9-[(1R,2S,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purine 
• 187877-40-3 Benzoic acid (1R,2R,3S,4S)-3,4-bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl ester 
• 187877-34-5 Benzoic acid (1S,2S,3S,4S)-3,4-bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl ester 
• 187877-75-4 9-[(1S,2S,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentyl]-6-chloro-9H-purin-2-ylamine 
• 187877-56-1 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1S-azido-2R-fluorocyclopentane 
• 187877-47-0 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1R-azido-2R-fluorocyclopentane 
• 187877-51-6 3S,4S-bis(t-butyldiphenylsilyloxymethyl)-1R-azido-2S-fluorocyclopentane 
• 187877-05-0 (1S,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanol 
• 187877-16-3 (1R,2R,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanol 
• 187877-11-8 (1S,2S,3S,4S)-3,4-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-2-fluoro-cyclopentanol 

Relevant academic research and scientific papers

Synthesis of 3',4'-C-bishydroxymethyl-2',3',4'-trideoxy-β-L-threo- pentopyranosyl nucleosides as potential inhibitors of HIV

The synthesis of 3',4'-bishydroxymethyl-2',3',4'-trideoxy pentopyranosyl derivatives of thymine, uracil, cytosine, and adenine is described. trans- (3S,4S)-Bis(methoxycarbonyl)cyclopentanone (3) was converted to 1-O-acetyl- 3,4-C-bis[(tert-butyldiphenylsiloxy)methyl]-2,3,4-trideoxy-α,β-L-threo- pentopyranose (6), which was subsequently condensed with the silylated purine and pyrimidine bases.

Synthesis of 2′,3′-dideoxycyclo-2′-pentenyl-3′-C-hydroxymethyl carbocyclic nucleoside analogues as potential anti-viral agents

The synthesis of optically pure unsaturated carbocyclic nucleoside analogues is described. (3,4S)-Bis(t-butyldiphenylsilyloxymethyl)-2-cyclopenten-1R and 1S-ol were coupled with 6-chloropurine and 2-amino-6-chloropurine respectively, using a modified Mits

Synthesis of novel olefinic carbocyclic purine nucleoside analogues

The synthesis of optically pure unsaturated carbocyclic nucleoside analogues is described. (3,4S)-Bis(t-butyldiphenyl silyloxymethyl)-1R and 1S cyclopent-2-en-1-ol were coupled with 6 chloropurine and 2-amino-6- chloropurine respectively, using a modified