Recent advances in alkyne-mediated cascade reactions enhance synthesis of carbocycles and heterocycles, indicating improved efficiency and diversity.
Carbocycles/Heterocycles are fundamental structural motifs in natural products, pharmaceuticals, and functional materials. Alkyne based cascade strategies have emerged as powerful tools for the efficient construction of these frameworks, enabling rapid access to diverse ring systems through domino cyclization pathways. This account highlights the representative recent advances of alkynemediated cascade reactions, covering transition-metal catalysis and acid-mediated reactions. These methods facilitate multiple bond forming events in a single operation, offering high atom and step economy. Special focus is given to illustrative transformations, mechanistic insights, and the broad utility of alkynes as precursors for the concise synthesis of diverse carbocyclic and heterocyclic molecular frameworks.
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Srinivas et al. (2025) studied this question.
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