Iridium-Catalyzed Intermolecular Asymmetric Dearomatization of β-Naphthols with Allyl Alcohols or Allyl Ethers

An Ir-catalyzed intermolecular asymmetric dearomatization reaction of beta-naphthols with allyl alcohols or allyl ethers was developed. When an iridium catalyst generated from [Ir(COD)Cl](2) (COD = cyclooctadiene) and a chiral P/olefin ligand is employed, highly functionalized beta-naphthalenone compounds bearing an all-carbon-substituted quaternary chiral center were obtained in up to 92% yield and 98% ee. The direct utilization of allyl alcohols as electrophiles represents an improvement from the viewpoint of atom economy. Allyl ethers were found to undergo asymmetric allylic substitution reaction under Ir catalysis for the first time. The diverse transformations of the dearomatized product to various motifs render this method attractive.