139212-86-5

Upstream product

• 127306-47-2 methyl-5-O-tert-butyldiphenylsilyl-2-deoxy-ribo-furanoside 
• 74-88-4 methyl iodide 

Downstream Products

• 145370-07-6 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-α-D-threo-pentofuranosyl)-5-pentyluracil 
• 145370-13-4 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-β-D-threo-pentofuranosyl)-5-pentyluracil 
• 145370-14-5 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-α-D-threo-pentofuranosyl)-5-hexyluracil 
• 145370-15-6 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-β-D-threo-pentofuranosyl)-5-hexyluracil 
• 139212-87-6 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-D-threo-pentafuranosyl)thymine 
• 176212-27-4 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-β-D-threo-pentofuranosyl)-2,4(1H,3H)-quinazolinedione 
• 202813-04-5 1-[(2S,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-decyloxymethyl-1H-pyrimidine-2,4-dione 
• 202813-08-9 1-[(2R,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-decyloxymethyl-1H-pyrimidine-2,4-dione 
• 202813-02-3 1-[(2S,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-heptyloxymethyl-1H-pyrimidine-2,4-dione 
• 202813-06-7 1-[(2R,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-heptyloxymethyl-1H-pyrimidine-2,4-dione 
• 202813-03-4 1-[(2S,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-octyloxymethyl-1H-pyrimidine-2,4-dione 
• 202813-07-8 1-[(2R,4R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-iodo-tetrahydro-furan-2-yl]-5-octyloxymethyl-1H-pyrimidine-2,4-dione 
• 3056-17-5 1-(2,3-dideoxy-D-glycero-pent-2-enofuranosyl)thymine 
• 139212-89-8 1-(5-O-tert-butyldiphenylsilyl-2,3-dideoxy-3-iodo-α-D-threo-pentofuranosyl)-5-(methoxymethyl)uracil 

Relevant academic research and scientific papers

Convergent Synthesis of 2',3'-Dideoxy-3'-methylthio and 2',3'-Dideoxy-3'-mercapto Nucleosides and their Disulfide Analogues - Potential Anti-HIV Agents

The iodide 4(α) or 7 synthesized in three steps from 2-deoxy-D-ribose 1, has been subjected to a number of nucleophilic substitution reactions producing the 3-benzoylthio-, 3-methylthio- and the 3-thiocyanato-2,3-dideoxy-D-erythro-pentofuranosides 8, 13 a