Abstract
Two novel tiazofurin analogues, 2-(2-benzamido-2-deoxy-β- d-ribofuranosyl)thiazole-4-carboxamide 4 and 2-(2-azido-2-deoxy-β- d-ribofuranosyl)thiazole-4-carboxamide 5 , have been synthesized starting from d-glucose and evaluated for their in vitro cytotoxicity against several human leukaemia and solid tumour cell lines.
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