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The vacuolar-type (H+)-adenosine triphosphatase inhibitor oximidine III and its enamide and epoxide stereoisomers have been synthesized enantioselectively. A relay ring-closing metathesis (RCM) strategy was employed to facilitate the macrocyclization of a well-defined substrate possessing two differentially functionalized RCM alkene partners (see scheme).
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Wang et al. (2004) studied this question.
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