Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions

Research output: Research - peer-reviewArticle

  • Authors:
  • Jacob Davies
  • Thomas D Svejstrup
  • Daniel Fernandez Reina
  • Nadeem S Sheikh
  • Daniele Leonori


The development of photoredox reactions of aryloxy-amides for the generation of amidyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported. Owing to the ease of single-electron-transfer reduction of the aryloxy-amides, the organic dye eosin Y was used as the photoredox catalyst, which results in fully transition-metal-free processes. These transformations exhibit a broad scope, are tolerant to several important functionalities, and have been used in the late-stage modification of complex and high-value N-containing molecules.

Bibliographical metadata

Original languageEnglish
Pages (from-to)8092-5
Number of pages4
JournalJournal of the American Chemical Society
Issue number26
StatePublished - 6 Jul 2016