Abstract
Despite the enormous developments in the asymmetric transformations of indole imine methides (IIMs), the remote asymmetric induction involving IIMs remains challenging due to the spatial interaction requirement between the substrate and catalyst. Herein we report the first catalytic asymmetric nucleophilic addition to indole imine 5-methide (5-IIM), the only topological isomer of IIMs whose asymmetric addition remains unknown. Considering the challenging remote stereocontrol, high efficiency and respectable enantioselectivity were achieved, providing access to a range of enantioenriched indole-containing triarylmethanes.
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Additional experimental and computational details, and spectroscopic data of all compounds
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