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- W3200480064 endingPage "25240" @default.
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- W3200480064 abstract "We report an approach for the intramolecular C(sp2 )-H amidation of N-acyloxyamides under photoredox conditions to produce δ-benzolactams with an aryl-alkyl σ-bond relocation. Computational studies on the designed reductive single electron transfer strategy led us to identify N-[3,5-bis(trifluoromethyl)benzoyl] group as the most effective amidyl radical precursor. Upon the formation of an azaspirocyclic radical intermediate by the selective ipso-addition with outcompeting an ortho-attack, radical-polar crossover was then rationalized to lead to the rearomative ring-expansion with preferential C-C bond migration." @default.
- W3200480064 created "2021-09-27" @default.
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- W3200480064 creator A5040227569 @default.
- W3200480064 creator A5060052469 @default.
- W3200480064 creator A5086637390 @default.
- W3200480064 date "2021-10-21" @default.
- W3200480064 modified "2023-10-14" @default.
- W3200480064 title "Visible‐Light Induced C(sp<sup>2</sup>)−H Amidation with an Aryl–Alkyl σ‐Bond Relocation via Redox‐Neutral Radical–Polar Crossover" @default.
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