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- W2155808546 endingPage "4059" @default.
- W2155808546 startingPage "4055" @default.
- W2155808546 abstract "A unified strategy involving visible-light-induced iminyl-radical formation has been established for the construction of pyridines, quinolines, and phenanthridines from acyl oximes. With fac-[Ir(ppy)3] as a photoredox catalyst, the acyl oximes were converted by 1 e− reduction into iminyl radical intermediates, which then underwent intramolecular homolytic aromatic substitution (HAS) to give the N-containing arenes. These reactions proceeded with a broad range of substrates at room temperature in high yield. This strategy of visible-light-induced iminyl-radical formation was successfully applied to a five-step concise synthesis of benzo[c]phenanthridine alkaloids." @default.
- W2155808546 created "2016-06-24" @default.
- W2155808546 creator A5007936773 @default.
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- W2155808546 creator A5040491864 @default.
- W2155808546 creator A5083586098 @default.
- W2155808546 creator A5086664284 @default.
- W2155808546 date "2015-02-03" @default.
- W2155808546 modified "2023-10-17" @default.
- W2155808546 title "Visible-Light-Promoted Iminyl-Radical Formation from Acyl Oximes: A Unified Approach to Pyridines, Quinolines, and Phenanthridines" @default.
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