139236-90-1

Upstream product

• 86528-49-6 2-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan 

Downstream Products

• 164666-91-5 Z-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-3-(4-hydroxy)anilino-2-propen-1-one 
• 143326-52-7 8-methyl-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3-dihydro-2H-1,5-benzodiazepin-2-one 
• 143326-51-6 7-methyl-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3-dihydro-2H-1,5-benzodiazepin-2-one 
• 143326-47-0 8-methyl-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one 
• 143326-46-9 7-methyl-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one 
• 143326-45-8 8-chloro-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one 
• 143326-43-6 7-chloro-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one 
• 146441-26-1 2-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)carbonyl>-2,3-dihydro-1,5-benzothiazepin-4(5H)-one 
• 146441-29-4 3-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5,6-dihydro-4H-1,4-thiazine-2-carboxaldehyde 
• 143326-44-7 7-chloro-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3-dihydro-2H-1,5-benzodiazepin-2-one 
• 143326-50-5 8-chloro-4-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)oxo>-1,3-dihydro-2H-1,5-benzodiazepin-2-one 
• 146441-27-2 2-<1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)carbonyl>-1,5-benzothiazepin-4(5H)-one 
• 151484-44-5 5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-isoxazole 
• 153751-21-4 methyl 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)quinoline-2-carboxylate 

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