Asymmetric hydrogenation of unsaturated ureas with the BIPI ligands

Org Lett. 2008 Jan 17;10(2):341-4. doi: 10.1021/ol7028542. Epub 2007 Dec 21.

Abstract

Asymmetric hydrogenation of unsaturated urea esters with the BIPI Ligands has been examined. Optimization of the P-N ligand structure has led to the development of chiral rhodium catalysts capable of producing the targets with >99% ee. The critical phosphine borane SNAr reaction needed for ligand synthesis has been optimized to give the adducts in high yield at ambient temperature with no racemization. An extremely concise, economical, and scalable sequence to these important new ligands for catalysis of asymmetric hydrogenation has been developed.

MeSH terms

  • Catalysis
  • Esters
  • Hydrogenation
  • Ligands
  • Molecular Structure
  • Phosphines / chemistry*
  • Rhodium / chemistry*
  • Stereoisomerism
  • Urea / analogs & derivatives*
  • Urea / chemistry*

Substances

  • Esters
  • Ligands
  • Phosphines
  • Urea
  • Rhodium