Enantioselective organocatalytic mannich reactions with autocatalysts and their mimics

J Org Chem. 2010 Apr 2;75(7):2403-6. doi: 10.1021/jo902500b.

Abstract

The Mannich reactions previously extensively investigated with organocatalysis of l-proline and other related small molecules were reinvestigated with detailed stereochemical analysis of their autocatalysis pathways, through employment of both the products themselves and their close structural mimics as the catalysts. These organo-autocatalytic processes function as meaningful molecular models toward understanding the origin and maintenance of homochirality under biologically relevant conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Chromatography, High Pressure Liquid
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Models, Molecular
  • Molecular Structure
  • Organometallic Compounds / chemistry*
  • Proline / chemistry*
  • Stereoisomerism
  • Zinc / chemistry*

Substances

  • Organometallic Compounds
  • Proline
  • Zinc