Metal-free iodine(III)-promoted synthesis of isoquinolones

J Org Chem. 2014 Nov 21;79(22):10988-98. doi: 10.1021/jo5020307. Epub 2014 Nov 10.

Abstract

A metal-free oxidative cycloaddition reaction of substituted benzamides and alkynes has been developed for the synthesis of isoquinolones by using bis(trifluoracetoxy)iodobenzene (PIFA) and trifluoroacetic acid (TFA). Under mild conditions, a wide variety of isoquinolones were conveniently prepared via oxidative annulation of simple N-methoxybenzamide and diarylacetylene or aryl/alkyl acetylene derivatives in yields up to 87%.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Catalysis
  • Cycloaddition Reaction
  • Iodine / chemistry*
  • Iodobenzenes / chemistry*
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / chemistry*
  • Metals / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Trifluoroacetic Acid / chemistry*

Substances

  • Alkynes
  • Iodobenzenes
  • Isoquinolines
  • Metals
  • Iodine
  • Trifluoroacetic Acid