1332330-06-9

Upstream product

• 157506-35-9 2,5-anhydro-3,6-di-O-methanesulfonyl-D-glucose ethylene acetal 
• 112-13-0 n-decanoyl chloride 
• 582-25-2 Potassium benzoate 
• 1332329-99-3 2,5-anhydro-4-O-n-decanoyl-3,6-di-O-methanesulfonyl-D-glucose ethylene acetal 
• 1332330-03-6 2,5-anhydro-3-azido-6-O-benzoyl-4-O-decanoyl-3-deoxy-D-allose ethylene acetal 
• 1332330-01-4 2,5-anhydro-6-O-benzoyl-4-O-decanoyl-3-O-methanesulfonyl-D-glucose ethylene acetal 

Downstream Products

• 1332330-08-1 2,5-anhydro-6-O-benzoyl-3-decanamido-3-deoxy-D-allonothioamide 
• 1332330-10-5 ethyl 2-(5-O-benzoyl-2-decanamido-2-deoxy-β-D-ribofuranosyl)thiazole-4-carboxylate 

Relevant academic research and scientific papers

Antitumour tiazofurin analogues embedded with an amide moiety at the C-2′ position

Synthesis of four new tiazofurin analogues has been accomplished starting from d-glucose. The key step of the synthesis was the three-step cascade that enabled an efficient hydrogen sulfide mediated one-pot conversion of 2-azido-3-O-acyl-ribofuranosyl cya