914983-68-9

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 
• 228399-13-1 2,5-anhydro-4-azido-3,6-di-O-benzoyl-4-deoxy-D-gulose ethylene acetal 
• 157506-35-9 2,5-anhydro-3,6-di-O-methanesulfonyl-D-glucose ethylene acetal 
• 914983-65-6 2,5-anhydro-3,6-di-O-benzoyl-4-deoxy-4-trifluoroacetamido-D-gulose ethylene acetal 
• 914983-67-8 C₂₂H₁₉F₃N₂O₇ 
• 914983-66-7 C₂₂H₁₈F₃NO₇ 

Downstream Products

• 914983-69-0 2,5-anhydro-3,6-di-O-benzoyl-4-deoxy-4-trifluoroacetamido-D-gulono-thioamide 

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

2-(3-Amino-3-deoxy-β-d-xylofuranosyl)thiazole-4-carboxamide: A new tiazofurin analogue with potent antitumour activity

A new tiazofurin analogue, 2-(3-amino-3-deoxy-β-d-xylofuranosyl)thiazole-4-carboxamide (3), was synthesized starting from d-glucose and evaluated for its in vitro antiproliferative activity against a panel of human tumour cell lines. Compound 3 exhibited