142468-64-2

Upstream product

• 142706-48-7 1-(3-deoxy-3-(phenylseleno)-β-D-arabinofuranosyl)uracil 
• 135824-30-5 1-<3-deoxy-3-(phenylseleno)-5-O-trityl-β-D-arabinofuranosyl>uracil 
• 1053735-65-1 C₃₃H₃₆N₂O₇SeSi 
• 142468-63-1 1-<2-O-acetyl-5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-(phenylseleno)-β-D-arabinofuranosyl>uracil 

Downstream Products

• 142560-93-8 4'-C-acetonyl-5'-O-(tert-butyldiphenylsilyl)-2',3'-didehydro-2',3'-dideoxyuridine 
• 142468-69-7 4'-C-acetonyl-5'-O-(tert-butyldiphenylsilyl)-2',3'-didehydro-2',3'-dideoxyuridine 
• 142468-71-1 5'-O-(tert-butyldiphenylsilyl)-4'-C-(1-oxocyclopent-2-yl)-2',3'-didehydro-2',3'-dideoxyuridine 
• 142468-71-1 5'-O-(tert-butyldiphenylsilyl)-4'-C-(1-oxocyclopent-2-yl)-2',3'-didehydro-2',3'-dideoxyuridine 
• 142468-67-5 1-[5-(tert-Butyl-diphenyl-silanyloxymethyl)-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 142468-65-3 1-[(2R,5S)-5-Allyl-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,5-dihydro-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 142560-91-6 1-[(2R,5R)-5-Allyl-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,5-dihydro-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 142560-94-9 5'-O-(tert-butyldiphenylsilyl)-2',3'-didehydro-2',3'-dideoxy-4'-C-phenacyluridine 
• 142468-70-0 5'-O-(tert-butyldiphenylsilyl)-2',3'-didehydro-2',3'-dideoxy-4'-C-phenacyluridine 
• 142468-72-2 5'-O-(tert-butyldiphenylsilyl)-4'-C-cyano-2',3'-didehydro-2',3'-dideoxyuridine 
• 142560-96-1 5'-O-(tert-butyldiphenylsilyl)-4'-C-cyano-2',3'-didehydro-2',3'-dideoxyuridine 
• 142560-92-7 1-[(2R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-5-(2-methyl-allyl)-2,5-dihydro-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 142468-68-6 1-[(2R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-5-(2-methyl-allyl)-2,5-dihydro-furan-2-yl]-1H-pyrimidine-2,4-dione 

Relevant academic research and scientific papers

Allylic substitution of 3′,4′-unsaturated nucleosides: Organosilicon-based stereoselective access to 4′-C-branched 2′,3′-didehydro-2′,3′-dideoxyribonucleosides

Reactions of organosilicon reagents (such as allyltrimethylsilane, silyl enol ethers, cyanotrimethylsilane) with 3′,4′-unsaturated nucleosides (of uracil, N4-acetylcytosine, and hypoxanthine) having an allyl ester structure were investigated in

Stereoselective synthesis of 4′-C-branched 2,′3′-didehydro-2′-dideoxy nucleosides based on SnCl4-promoted allylic rearrangement

Based on SnCl4-[promoted allylic rearrangement between a 3′,4′-unsaturated uracil nucleoside and organosilicon reagents, stereoselective introduction of carbon functionalities to the 4′-position has been accomplished, disclosing a new entry for