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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