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ChemInform Abstract: Synthesis and Biological Evaluation of a Series of 2′-Fluorinated-2′,3′-dideoxy-2′,3′-didehydro-(L)-nucleosides.

✍ Scribed by S.-H. CHEN; Q. WANG; J. MAO; I. KING; G. E. DUTSCHMAN; E. A. GULLEN; Y.-C. CHENG; T. W. DOYLE


Publisher
John Wiley and Sons
Year
2010
Weight
37 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis


Synthesis and Biological Evaluation of a Series of 2'-Fluorinated-2',3'-dideoxy-2',3'-didehydro-(L)-nucleosides.

-A general method for the synthesis of both the cis-and trans-2'-vinylfluoro containing nucleosides is presented. Among the nucleosides prepared compound (XI) displays the best biological activity. Interestingly, the incorporation of a fluorine atom at the 2'-position improves the cytotoxicity profile at the nucleoside, but fails to enhance its antiviral activity.


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