C7-Sulfonamide Functionalization of 7-Deazaadenosines: Sangivamycin Analogues with Haspin Inhibitory Activity
Abstract
We report a robust method for C7-sulfonamide installation on 7-deazaadenosines, enabled by an unprecedentedly stable sulfonyl chloride. This general transformation introduces a new functionalization site and expands nucleoside chemical space, offering a powerful platform for constructing tailored probes and analogues in synthetic and bioorganic chemistry.
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