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Summary. In order to design potential inhibitors of UDP-glucuronosyltransferase, two different pathways for the synthesis of cyclohexane containing 5'-O-glycine derivatives of uridine were developed, one starting with the cyclohexyl moiety, and a second one beginning with the uridine moiety. Thus, 5'-O-(cyclohexylcarboxyl-glycyl)-2',3'-O-isopropylideneuridine and 5'-O-(cyclohexylpropionyl-glycyl)-2',3'-O-isopropylideneuridine were obtained. According to the results, the second approach is more convenient.