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3‐Fluorosialosyl fluorides are inhibitors of sialidases that function by the formation of a long‐lived covalent active‐site adduct and have potential as therapeutics if made specific for the pathogen sialidase. Surprisingly, human Neu2 and the Trypanosoma cruzi trans‐sialidase are inactivated more rapidly by the reagent with an equatorial fluorine at C3 than by its axial epimer, with reactivation...
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