Review summarizes radical C3-alkylation methodologies for coumarins, highlighting implications for molecular diversity and bioactivity.
High Resolution Image Download MS PowerPoint Slide Radical chemistry has emerged as a powerful platform for the construction of carbon–carbon and carbon–heteroatom bonds under mild and operationally simple conditions. In this context, the direct functionalization of heterocyclic scaffolds has attracted significant attention because of its potential for rapid molecular diversification and late-stage modification of bioactive compounds. Among these scaffolds, coumarins occupy a prominent position owing to their widespread occurrence in natural products, pharmaceuticals, and functional materials. Although classical approaches have enabled efficient access to coumarin cores, the direct and selective functionalization of the C3 position remains a significant challenge. In recent years, radical-based methodologies have become powerful and versatile strategies for overcoming this limitation, allowing efficient C3-alkylation of coumarins without the requirement for prefunctionalized substrates. This review provides a comprehensive overview of recent advances in the radical-mediated C3-alkylation of coumarins. The discussion is organized according to the activation mode, highlighting key developments in thermal and photoredox strategies. Emphasis is placed on mechanistic aspects, substrate scope, and synthetic applicability, offering a critical perspective on the advantages and limitations associated with each approach. Finally, emerging trends and future opportunities for the development of more efficient, selective, and sustainable methodologies for C3-functionalization of coumarins are discussed.
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Caiuby et al. (2026) studied this question.
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