259256-59-2

Upstream product

• 259256-57-0 9-[5-O-(tert-butyldiphenylsilyl)-3-deoxy-2-Se-phenyl-2-seleno-β-L-erythro-pentofuranosyl]-6-chloro-2-fluoro-9H-purine 
• 128075-94-5 (R)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}dihydrofuran-2(3H)-one 
• 190078-48-9 (3R,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-phenylselanyl-dihydro-furan-2-one 
• 189818-62-0 5-O-(tert-butyldiphenylsilyl)-3-deoxy-2-Se-phenyl-2-seleno-L-erythro-pentonic acid-γ-lactone 
• 189818-64-2 1-O-acetyl-5-O-(tert-butyldiphenylsilyl)-3-deoxy-2-Se-phenyl-2-seleno-α-and-β-L-erythro-pentofuranose 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 52813-63-5 (5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone 

Downstream Products

• 259261-21-7 9-[5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-β-L-glycero-pentofuranosyl]-2-fluoroadenine 
• 259261-20-6 9-[5-O-(tert-butyldiphenylsilyl)-2,3-deoxy-β-L-glycero-pent-2-enofuranosyl]-2-fluoroadenine 

Relevant academic research and scientific papers

Stereoselective synthesis of β-L-2',3'- dideoxy- and L-2',3'- didehydro-2',3'-dideoxy purine nucleosides

β-L-2',3'-Dideoxy- and L-2',Y-didehydro-2',Y-dideoxy purine nucleosides have been synthesized via a highly stereoselective method of glycosylation by the condensation of L-2-(phenylselenyl)-2,3-dideoxyribose derivative with silylated heterocyclic base.