108007-65-4

Upstream product

• 108007-59-6 5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-furoic acid 
• 108007-59-6 5-(2,3,5-tri-O-benzoyl-α-D-ribofuranosyl)-2-furoic acid 
• 108007-57-4 5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-furancarboxaldehyde 
• 108007-58-5 5-(2,3,5-tri-O-benzoyl-α-D-ribofuranosyl)-2-furancarboxaldehyde 
• 108007-63-2 tert-butyl N-<5-(2,3,5-tri-O-benzoyl-β-ribofuranosyl)-2-furyl>carbamate 
• 86528-49-6 2-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan 
• 108007-64-3 N-(tert-butoxycarbonyl)-5-hydroxy-5-(2,3,5,-tri-O-benzoyl-β-D-ribofuranosyl)-3-pyrrolin-2-one 
• 86528-50-9 2-(2,3,5-tri-O-benzoyl-α-D-ribofuranosyl)furan 

Downstream Products

• 108007-66-5 5-methoxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-3-pyrrolin-2-one 

Relevant academic research and scientific papers

C-Nucleosides. 6. Synthesis of 5-Methoxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan-2(5H)-one and Its Ring Transformation

Synthesis of the versatile and stable C-nucleoside precursor 5-hydroxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan-2(5H)-one (2) was achieved by oxidation of glycosyl furan (1) with Jones reagent.Treatment of 2 with triethylamine in benzene afforded th

C-Nucleosides. 5. Synthesis of 5-Hydroxy-5-(β-D-ribofuranosyl)-3-pyrrolin-2-one from Glycosylfuran

Synthesis of 5-hydroxy-5-(β-D-ribofuranosyl)-3-pyrrolin-2-one (18) from 2-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl) furan (3) is described.Treatment of β- and α-azido compounds 9 and 10 with tert-butyl alcohol in benzene afforded only tert-butyl N-5-(2,3,5