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Demonstrates a new way to create 2-quinolinones using ethanol, suggesting an innovative approach to green chemistry.
Ethanol, a widely available, low-cost, and environmentally friendly biomass-derived platform molecule, holds untapped potential beyond its conventional use as a solvent. Herein, we report a visible-light-induced hydrogen atom transfer approach that harnesses ethanol’s dual function as a mediator and green solvent to accomplish the formal ring-closing metathesis of o -cyano and o -alkynyl acrylamides. This transition metal- and oxidant-free protocol provides efficient access to biologically important 2-quinolinones. Mechanistic studies support a pathway in which ethanol mediates key C=C bond cleavage via an in-situ-generated α-hydroxyethyl radical, and a plausible reaction mechanism for this transformation is proposed.
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Yu et al. (2026) studied this question.
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