605674-46-2

Upstream product

• 99-56-9 4-Nitrophenylene-1,2-diamine 
• 50908-40-2 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythropentofuranosyl 1-cyanide 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 

Downstream Products

• 605674-39-3 C₂₈H₂₅N₃O₇ 

Relevant academic research and scientific papers

A short and efficient synthesis of 2′-deoxybenzo- and pyridoimidazole C-nucleosides

A short route to a series of 2′-deoxy-C-nucleosides featuring substituted nucleobases has been developed. The key step is the formation of the cyclized products following Mukaiyama's type amide coupling and a simple dehydration, starting from readily accessible synthons. The epimerization of the C1′-stereogenic center was avoided under mild and controlled conditions.