210548-19-9

Upstream product

• 218601-09-3 Benzoic acid (3R,4R,5S)-4-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-3-yl ester 

Downstream Products

• 218601-09-3 Benzoic acid (3R,4R,5S)-4-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-3-yl ester 
• 287724-99-6 Benzoic acid (3S,4R,5S)-4-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-3-yl ester 
• 218601-14-0 Benzoic acid (3R,4R,5S)-4-hydroxy-5-hydroxymethyl-tetrahydro-thiophen-3-yl ester 
• 218601-17-3 Benzoic acid (3R,4R,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-4-hydroxy-tetrahydro-thiophen-3-yl ester 
• 218601-31-1 9-[(3R,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-yl]-6-chloro-9H-purine 
• 218601-29-7 3-Benzoyl-1-[(3R,4R,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-yl]-1H-pyrimidine-2,4-dione 
• 218601-27-5 (3S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-ol 
• 218601-22-0 (3R,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-ol 
• 218601-25-3 Benzoic acid (3S,4R,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-yl ester 
• 218601-19-5 Benzoic acid (3R,4R,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-4-fluoro-tetrahydro-thiophen-3-yl ester 
• 211616-60-3 1-((3R,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-3-fluoro-tetrahydro-thiophen-2-yl)-5-methyl-1H-pyrimidine-2,4-dione 
• 210548-23-5 N-[1-((2R,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-3,3-difluoro-tetrahydro-thiophen-2-yl)-2-oxo-1,2-dihydro-pyrimidin-4-yl]-benzamide 
• 210548-24-6 N-[1-((2S,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-3,3-difluoro-tetrahydro-thiophen-2-yl)-2-oxo-1,2-dihydro-pyrimidin-4-yl]-benzamide 
• 210548-37-1 N-[1-((2R,4R,5S)-3,3-Difluoro-4-hydroxy-5-hydroxymethyl-tetrahydro-thiophen-2-yl)-2-oxo-1,2-dihydro-pyrimidin-4-yl]-benzamide 

Relevant academic research and scientific papers

A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents

L-β-2′-Deoxy-4′-thio-1′-purine nucleosides were synthesized efficiently utilizing the neighboring group effect of the 2-benzoyl-4-thiosugar acetate. The Royal Society of Chemistry 2000.

Ring contraction and rearrangement of 4-thiofuranose derivatives observed during dast fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine

Ring contraction and rearrangement of 4-thiofuranose derivatives were observed through the regioselective opening of the episulfonium ion formed during DAST fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine.