Heteroatom-directed Wacker oxidations. A protection-free synthesis of (−)-heliophenanthrone

Abstract

The first enantioselective six-step synthesis of (−)-heliophenanthrone has been achieved without any protection–deprotection protocol at an overall yield of 28%. Key features of this synthesis comprise a heteroatom-directed Wacker oxidation of an internal cyclic olefin in addition to asymmetric Brown allylation and ring closing metathesis (RCM).