Demonstrates a novel method to access arylthiobutyraldehydes and arylthiobutanols, highlighting its synthetic utility.
We report a base/acid-controlled oxidative ring opening of sulfonium salts that delivers, in a switchable and selective manner, two distinct classes of S-containing linear products, arylthiobutyraldehydes and arylthiobutanols. The transformation proceeds under operationally simple conditions and exhibits a broad substrate scope and high functional group tolerance. In addition, sulfonium salts can be directly engaged in one-pot coupling/annulation with 2-(1H-pyrrol-1-yl)anilines to furnish sulfur-containing pyrrolo[1,2-a]quinoxaline derivatives. The resulting products are readily diversified to sulfoxides, sulfones, sulfoximines, and additional heterocyclic scaffolds, demonstrating the synthetic utility of this platform.
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An et al. (2026) studied this question.
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