Total Synthesis of (+)-Antroquinonol and (+)-Antroquinonol D

The first total synthesis of (+)-antroquinonol and (+)-antroquinonol D, two structurally unique quinonols with a sesquiterpene side chain, is described. The route features an iridium-catalyzed olefin isomerization-Claisen rearrangement reaction (ICR), lactonization, and Grubbs olefin metathesis. The requisite alpha,beta-unsaturation was achieved via the selenylation/oxidation protocol and elimination of beta-methoxy group to provide two natural products from a common intermediate.