Synthesis of highly functionalized polycyclic quinoxaline derivatives using visible-light photoredox catalysis

Angew Chem Int Ed Engl. 2014 Dec 22;53(52):14451-5. doi: 10.1002/anie.201408522. Epub 2014 Oct 27.

Abstract

A mild and facile method for preparing highly functionalized pyrrolo[1,2-a]quinoxalines and other nitrogen-rich heterocycles, each containing a quinoxaline core or an analogue thereof, has been developed. The novel method features a visible-light-induced decarboxylative radical coupling of ortho-substituted arylisocyanides and radicals generated from phenyliodine(III) dicarboxylate reagents and exhibits excellent functional group compatibility. A wide range of quinoxaline heterocycles have been prepared. Finally, a telescoped preparation of these polycyclic compounds by integration of the in-line isocyanide formation and photochemical cyclization has been established in a three-step continuous-flow system.

Keywords: flow chemistry; heterocycles; isocyanide; photochemistry; radicals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cyanides / chemistry
  • Cyclization
  • Light*
  • Oxidation-Reduction
  • Polycyclic Compounds / chemistry*
  • Pyrroles / chemical synthesis
  • Pyrroles / chemistry*
  • Quinoxalines / chemical synthesis
  • Quinoxalines / chemistry*

Substances

  • Cyanides
  • Polycyclic Compounds
  • Pyrroles
  • Quinoxalines
  • pyrrolo(1,2-a)quinoxaline