Synthesis and antiviral evaluation of 2′,2′,3′,3′-tetrafluoro nucleoside analogs
文摘
The synthesis of novel 2′,2′,3′,3′-tetrafluoro nucleoside analogs is described. Glycosylation reactions are achieved via Mitsunobu coupling. Energetics of ring conformation are compared to differently substituted ribose. Evaluation of Tetrafluoro nucleosides in vitro against a panel of DNA and RNA viruses.