| Autor: |
Hornink, Milene M., Figlino, Giuseppe E., Toledo, Mônica F. Z. J., Pimenta, Daniel C., Stefani, Hélio A. |
| Zdroj: |
Organic Letters; October 2024, Vol. 26 Issue: 40 p8621-8625, 5p |
| Abstrakt: |
Cascade reactions are important synthetic tools for the synthesis of heterocyclic molecules, particularly those catalyzed by palladium. Herein, we report a palladium-catalyzed aminocarbonylative cyclization of new 1-alkynyl-2-iodo-d-glucals, which undergo a tandem carbonylative cyclization in the presence of various amine nucleophiles. A broad range of aromatic and aliphatic amines were applied as coupling partners, resulting in the selective and high-yield synthesis of glycosides fused to pyridinones. A plausible mechanism is proposed, proceeding via a tandem palladium aminocarbonylation followed by a palladium-catalyzed endo-digcyclization. |
| Databáze: |
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