Catalytic Enantioselective Desymmetrizing Fischer Indolization through Dynamic Kinetic Resolution

Abstract The first catalytic enantioselective Fischer indolization of prochiral diketones containing enantiotopic carbonyl groups is developed and shown to proceed through dynamic kinetic resolution (DKR). Catalyzed by the combination of a spirocyclic chiral phosphoric acid and ZnCl 2 (Lewis acid assisted Brønsted acid), this direct approach combines 2,2‐disubstituted cyclopentane‐1,3‐diones with N ‐protected phenylhydrazines to furnish cyclopenta[ b ]indole derivatives containing an all‐carbon quaternary stereocenter with good to excellent enantioselectivities.