Asymmetric Synthesis of Remotely Chiral Naphthols and Naphthylamines via Naphthoquinone Methides

Quinone methides are well-established intermediates in asymmetric synthesis. In contrast, their extended analogues with the carbonyl and methide units distributed across two different rings have not been exploited in asymmetric synthesis. Herein, we achieved the first asymmetric process involving such intermediates. Specifically, the use of suitable chiral phosphoric acids enabled in situ generation of 2-naphthoquinone 8-methides and the corresponding aza counterparts for mild one-pot asymmetric nucleophilic addition. These processes provided rapid access to a wide range of previously less accessible remotely chiral naphthols and naphthylamines with both high efficiency and excellent enantioselectivity. Control experiment and DFT calculations provided important insights into the reaction mechanism, which likely involves two phosphoric acid molecules in the enantiodetermining transition states. This work serves as a proof of concept for the exploitation of new types of extended quinone methides as versatile intermediates for asymmetric synthesis, thus providing a new platform for the efficient construction of remote benzylic stereogenic centers of aromatic compounds.