Regioselective Thionation at C-2 of N-Substituted Isatins: Overcoming Synthetic Paradigms

Abstract

This work employs Lawesson's reagent under simple operational conditions and short reaction times to selectively introduce sulfur at C-2 in isatin, enabling access to a diverse range of 2-thioisatins. It fills a decades-long gap in isatin chemistry, allowing the synthesis of a new class of heterocycles and challenging the inherent reactivity of C-3.

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Article information

Article type
Communication
Submitted
12 Dec 2025
Accepted
07 Apr 2026
First published
16 Apr 2026

New J. Chem., 2026, Accepted Manuscript

Regioselective Thionation at C-2 of N-Substituted Isatins: Overcoming Synthetic Paradigms

S. Cubas, H. Santos, M. T. Rodrigues Jr, L. A. Zeoly and F. Coelho, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D5NJ04805B

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