Abstract
AbstractThe reaction of D‐ribose tosylate (I) with allyl amine followed by a Cu‐catalyzed reaction with terminal alkynes (III) gives rise to new iminosugar β‐C‐alkynylglycosides (IV), which are readily converted into novel 1‐vinyl‐tetrahydroindolizine DNA‐cross‐linking agents (V).
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