Dearomatization–scission–aromatization of anilines: En route to synthesis of 3,3-disubstituted oxindoles with a wide range of heteroatom nucleophiles

Abstract

Herein, we report a catalytic, redox-neutral method for the difunctionalization of oxindoles using ketimines derived from anilines and heteronucleophiles. The reaction proceeds through a dearomatization–aromatization strategy via a tetra-substituted alkene intermediate stabilized by extended resonance, facilitating the selective formation of 3,3-disubstituted oxindoles with a wide chemical space in good-to-high yields.

Graphical abstract: Dearomatization–scission–aromatization of anilines: En route to synthesis of 3,3-disubstituted oxindoles with a wide range of heteroatom nucleophiles

Supplementary files

Article information

Article type
Communication
Submitted
25 Apr 2025
Accepted
25 Jul 2025
First published
30 Jul 2025

Chem. Commun., 2025, Advance Article

Dearomatization–scission–aromatization of anilines: En route to synthesis of 3,3-disubstituted oxindoles with a wide range of heteroatom nucleophiles

P. Jha, S. Husen, S. Sinha and R. Kumar, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D5CC02309B

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