4.8 Article

Photoredox-Induced Three-Component Oxy-, Amino-, and Carbotrifluoromethylation of Enecarbamates

Journal

ORGANIC LETTERS
Volume 16, Issue 4, Pages 1240-1243

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol500374e

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Funding

  1. ICSN
  2. CNRS
  3. Labex Charmmmat

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A photoredox-catalzyed trifluoromethylation of enecarbamates process is reported. This pathway uses Togni's reagent as the CF3 source and follows a radical/cationic pathway. Under the optimized conditions using [Ru(bpy)(3)(PF6)(2)] as the photocatalyst, a wide range of substituted enecarbamates can readily be difunctionalized by means of various O, N, and C nudeophiles.

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