Recyclable Merrifield resin-supported organocatalysts containing pyrrolidine unit through A3-coupling reaction linkage for asymmetric Michael addition

Chirality. 2010 May 5;22(4):432-41. doi: 10.1002/chir.20759.

Abstract

Merrifield resin-supported pyrrolidine-based chiral organocatalysts A-D through A(3)-coupling reaction linkage have been developed and found to be highly effective catalysts for the Michael addition reaction of ketones with nitrostyrenes. The reactions generated the corresponding products in good yields (up to 92%), excellent enantioselectivities (up to 98% ee), and high diastereoselectivities (up to 99:1 dr). In addition, the catalysts can be reused at least five times without a significant loss of catalytic activity and stereoselectivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Chemistry, Organic / methods
  • Chromatography, High Pressure Liquid / methods
  • Ketones / chemistry
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Polystyrenes / chemistry*
  • Pyrrolidines / chemistry*
  • Solvents
  • Spectrophotometry / methods
  • Stereoisomerism
  • Styrenes / chemistry*
  • Toluene / chemistry

Substances

  • Ketones
  • Merrifield resin
  • Polystyrenes
  • Pyrrolidines
  • Solvents
  • Styrenes
  • Toluene
  • pyrrolidine