109930-06-5

Upstream product

• 86528-49-6 2-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan 
• 139236-90-1 5-hydroxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranozyl)-furan-2(5H)-one 

Downstream Products

• 128745-68-6 4-(3,5-di-O-benzoyl-2-deoxy-β-D-erythro-pentofuranosyl)-4-oxobutyric acid 
• 128745-69-7 4-(3,5-di-O-benzoyl-2-deoxy-α-D-erythro-pentofuranosyl)-4-oxobutyric acid 
• 128745-71-1 methyl 4-(3,5-di-O-benzoyl-2-deoxy-α-D-erythro-pentofuranosyl)-4-oxobutyrate 
• 128745-70-0 methyl 4-(3,5-di-O-benzoyl-2-deoxy-β-D-erythro-pentofuranosyl)-4-oxobutyrate 
• 128745-75-5 3-(3,5-di-O-benzoyl-2-deoxy-α-D-erythro-pentofuranosyl)pyridazin-6(1H)-one 
• 128745-74-4 3-(3,5-di-O-benzoyl-2-deoxy-β-D-erythro-pentofuranosyl)pyridazin-6(1H)-one 
• 128745-73-3 3-(3,5-di-O-benzoyl-2-deoxy-α-D-erythro-pentofuranosyl)-4,5-dihydropyridazin-6(1H)-one 
• 128745-72-2 3-(3,5-di-O-benzoyl-2-deoxy-β-D-erythro-pentofuranosyl)-4,5-dihydropyridazin-6(1H)-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