Visible-Light-Induced Cascade Reaction of Isocyanides and N-Arylacrylamides with Diphenylphosphine Oxide via Radical C–P and C–C Bond Formation

An effective photoredox-mediated tandem phosphorylation/cyclization reaction of diphenylphosphine oxide with three types of radical acceptors leads to P(O)Ph₂-containing phenanthridines, isoquinolines, and indolin-2-ones by formation of both C-P and C-C bonds. [Ir(ppy)₂(dtbpy)]PF₆ (1 mol %) was used as the catalyst, CsF or Cs₂CO₃ as the base, and K₂S₂O₈ as the oxidant. A series of functional groups can be tolerated at room temperature. Moderate to good yields were generated.