Dearomatization-Scission-Aromatization of Anilines: En route to Synthesis of 3,3-Disubstituted Oxindoles with Wide 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 dearomatization-aromatization strategy via tetra-substituted alkene intermediate stabilized by extended resonance, facilitating the selective formation of 3,3-disubstituted oxindoles with wide chemical space in good to high yields.

Supplementary files

Article information

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

Chem. Commun., 2025, Accepted Manuscript

Dearomatization-Scission-Aromatization of Anilines: En route to Synthesis of 3,3-Disubstituted Oxindoles with Wide Heteroatom Nucleophiles

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

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