Total Synthesis of (+)‐Dendrowardol C

Abstract

Abstract The first total synthesis of the tetracyclic sesquiterpenoid (+)‐dendrowardol C is described. It relies on an intramolecular aldol reaction to forge the central bicyclic scaffold and subsequent cyclobutane formation by cyclization of a γ‐triflyloxy ketone. Key is the treatment of the latter with lithium naphthalenide. Finally, the diastereoselective hydroboration of a 1,1‐disubstituted double bond is enabled by a chiral Co I catalyst.