Abstract
Norrisolide (1) belongs to a family of marine diterpenes that are characterized by the assembly of a bicyclic core with a unique and highly oxygenated side chain (norrisane side chain). As a prelude to the synthesis of 1, we present herein a short, efficient, and enantioselective synthesis of the norrisane side chain 4. The synthetic route toward 4 departs from d-mannose and is short (11 steps), efficient, and enantioselective.
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