N-Substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-H amidation reaction

Org Lett. 2014 Jun 20;16(12):3328-31. doi: 10.1021/ol501338h. Epub 2014 Jun 5.

Abstract

N-Substituted hydroxylamines such as aroyloxy- or acyloxycarbamates were successfully employed as synthetically versatile amino precursors in the iridium-catalyzed direct C-H amidation of arenes. The reaction proceeds smoothly at room temperature over a broad range of substrates with high functional group tolerance to afford N-substituted arylamine products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • Carbamates / chemistry
  • Catalysis
  • Hydroxylamines / chemistry*
  • Iridium / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Amides
  • Carbamates
  • Hydroxylamines
  • Iridium