ArticleAngewandte Chemie (International ed. in English)2025
Ligand-Controlled Chemoselectivity in the Rhodium-Catalyzed Synthesis of Pentafulvenes via (2 + 2 + 1) Alkyne Cyclotrimerization.
Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- Ligand-Controlled Chemoselectivity in the Rhodium-Catalyzed Synthesis of Pentafulvenes via (2 + 2 + 1) Alkyne Cyclotrimerization.Angewandte Chemie (International ed. in English) · 2025Article
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7 authors.
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Abstract
The synthesis of pentafulvenes with varied substituents has been efficiently achieved using novel rhodium-based catalysts via (2 + 2 + 1) alkyne cyclotrimerization. A rational design of the catalyst structure, including pyridonato, NHC, and CO ligands, ensures the alkyne chemoselectivity and prevents the formation of robust rhodium-fulvene species. Furthermore, the judicious choice of acidity and steric properties of different alkynes enables the preparation of cross-coupled fulvene derivatives. Stoichiometric and deuteration experiments, as well as DFT calculations, shed light on the reaction mechanism, showing that it includes an initial alkyne deprotonation, two successive alkyne insertions, cyclization, and protonolysis, the first insertion being the rate-determining step.
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