615249-48-4

Upstream product

• 98-88-4 benzoyl chloride 
• 258336-08-2 Benzoic acid (1R,2R,4R,5R)-4-[1,3]dioxolan-2-yl-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethyl ester 
• 108-24-7 acetic anhydride 
• 228399-13-1 2,5-anhydro-4-azido-3,6-di-O-benzoyl-4-deoxy-D-gulose ethylene acetal 

Downstream Products

• 615249-50-8 C₂₂H₂₁NO₇ 
• 615249-51-9 C₂₂H₂₂N₂O₇ 
• 615249-52-0 (3-acetamido-2,5-di-O-benzoyl-3-deoxy-β-D-xylofuranosyl)cyanide 
• 615249-53-1 4-acetamido-2,5-anhydro-3,6-di-O-benzoyl-4-deoxy-D-gulono-thioamide 
• 615249-54-2 ethyl 2-(3-acetamido-2,5-di-O-benzoyl-3-deoxy-β-D-xylofuranosyl)thiazole-4-carboxylate 

Relevant academic research and scientific papers

Structure based design, synthesis and in vitro antitumour activity of tiazofurin stereoisomers with nitrogen functions at the C-2′ or C-3′ positions

Three novel tiazofurin analogues having D-arabino stereochemistry and nitrogen functionalities at the C-2′ position (5–7) have been designed and synthesized in multistep sequences, starting from D-glucose. The known D-xylo stereoisomer of 1 (compound 2) a

De novo synthesis of two new cytotoxic tiazofurin analogues with modified sugar moieties

A divergent synthesis of two novel tiazofurin analogues, 2-(3-deoxy-3-fluoro-β-D-xylofuranosyl)thiazole-4-carboxamide (2) and 2-(3-acetamido-3-deoxy-β-D-xylofuranosyl)thiazole-4-carboxamide (3), has been achieved starting from D-glucose. Both nucleoside a