Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization

Abstract

Abstract A concise, protecting‐group‐free total synthesis of the unusual brominated sesquiterpene aplydactone is described. Our synthesis features a [2+2] photocycloaddition, a Wolff ring contraction, an unusual remote C−H functionalization to establish the highly strained tetracyclic core, and a hydrogen‐atom transfer (HAT) reaction to access the bromine‐containing stereocenter. A finely tuned conformation of the α‐diazoketone precursor is the key for the success of the late‐stage transannular C−H insertion to deliver a bridged six‐membered ring and a quaternary stereocenter (C6) between two quaternary carbon atoms (C1 and C7).