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- W4308954670 abstract "A rhodium(III)-catalyzed Satoh-Miura type oxidative annulation of N-aryl 2-pyridone derivatives is described using internal alkyne as a coupling partner. A weakly coordinating carbonyl group of the 2-pyridone ring is utilized for this transformation. The reaction proceeds with a broad scope and wide functional group tolerance. The solvent plays an important role in the developed method to furnish a different class of annulated product. A preliminary investigation was carried out to explore the photophysical properties of the obtained polyarylated N-naphthyl 2-pyridones." @default.
- W4308954670 created "2022-11-20" @default.
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- W4308954670 date "2022-11-14" @default.
- W4308954670 modified "2023-09-28" @default.
- W4308954670 title "Rh(III)-Catalyzed Weakly Coordinating 2-Pyridone-Directed Oxidative Annulation Using Internal Alkynes: A Reversal in Selectivity" @default.
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- W4308954670 doi "https://doi.org/10.1021/acs.orglett.2c03187" @default.
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