Double diastereoselective SuperQuat glycolate aldol reactions: application to the asymmetric synthesis of polyfunctionalised lactones

Org Biomol Chem. 2004 Nov 21;2(22):3385-400. doi: 10.1039/B411724G. Epub 2004 Oct 11.

Abstract

Polyfunctionalised lactones with up to five contiguous stereocentres may be prepared with high stereocontrol by a double diastereoselective aldol protocol with protected homochiral alpha,beta-dihydroxy- or alpha,beta-gamma-trihydroxyaldehydes and a chiral glycolate oxazolidinone, followed by subsequent O-desilylation and lactonisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry*
  • Chemistry, Organic / methods*
  • Glycolates / chemistry*
  • Lactones / chemical synthesis*
  • Lactones / chemistry
  • Lactones / metabolism
  • Models, Chemical
  • Stereoisomerism

Substances

  • Aldehydes
  • Glycolates
  • Lactones
  • glycolic acid
  • 3-hydroxybutanal