Highly enantioselective iridium-catalyzed hydrogenation of heteroaromatic compounds, quinolines

J Am Chem Soc. 2003 Sep 3;125(35):10536-7. doi: 10.1021/ja0353762.

Abstract

The highly enantioselective hydrogenation of quinoline derivatives is developed using [Ir(COD)Cl]2/(R)-MeO-Biphep/I2 system, and this methodology has been applied to the asymmetric synthesis of three naturally occurring alkaloids angustureine, galipinine, and cuspareine. This method provided an efficient access to a variety of optically active tetrahydroquinolines with up to 96% ee.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Hydrogenation
  • Iridium / chemistry*
  • Organometallic Compounds / chemistry
  • Quinolines / chemical synthesis
  • Quinolines / chemistry*
  • Stereoisomerism

Substances

  • Organometallic Compounds
  • Quinolines
  • Iridium