Asymmetric synthesis of methylenetetrahydrofurans by palladium-catalyzed [3 + 2] cycloaddition of trimethylenemethane with aldehydes--a novel ligand design

J Am Chem Soc. 2011 May 25;133(20):7664-7. doi: 10.1021/ja201181g. Epub 2011 May 3.

Abstract

The palladium-catalyzed [3 + 2] cycloaddition of trimethylenemethane (TMM) with aldehydes is a direct and efficient route to methylenetetrahydrofurans. Herein we describe the first asymmetric synthesis of methylenetetrahydrofurans utilizing a palladium-TMM complex in the presence of a novel phosphoramidite ligand possessing a stereogenic phosphorus. The method allows for the formation of chiral disubstituted tetrahydrofurans in good yields and enantioselectivities.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aldehydes / chemistry*
  • Catalysis
  • Chromatography, High Pressure Liquid
  • Ligands
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Palladium / chemistry*

Substances

  • Aldehydes
  • Ligands
  • trimethylenemethane
  • Palladium
  • Methane