Catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters: application to 1,3-polyol/alpha-pyrone natural product synthesis

Org Lett. 2003 Feb 20;5(4):495-8. doi: 10.1021/ol0273708.

Abstract

[reaction: see text] We describe a catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters. The method relies upon catalytic asymmetric epoxidation of alpha,beta-unsaturated imidazolides and amides, using lanthanide-BINOL complexes, and diastereoselective reduction of ketones. The method was applied to the enantioselective syntheses of 1,3-polyol/alpha-pyrone natural products 9a, 9b, and strictifolione (10). The absolute stereochemistry of 9a and 9b was also determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Factors / chemical synthesis
  • Catalysis
  • Esters / chemical synthesis*
  • Hydroxy Acids / chemical synthesis*
  • Pyrones / chemistry
  • Stereoisomerism

Substances

  • Biological Factors
  • Esters
  • Hydroxy Acids
  • Pyrones