Addition of dithiols to bis-ynones: development of a versatile platform for the synthesis of polyketide natural products

Org Lett. 2003 Apr 3;5(7):1147-50. doi: 10.1021/ol034248f.

Abstract

[reaction: see text] The conjugate addition of dithiols to bis-ynones generates a versatile masked 1,3,5-triketone platform. These functional units are useful intermediates for the synthesis of oxygen-containing heterocycles commonly found in polyketide natural products. The tetrahydropyranyl fragments of the marine macrolides Lyngbouilloside and Callipeltoside A have been synthesized with use of this methodology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Biological Products / chemical synthesis*
  • Biological Products / chemistry
  • Glycosides / chemical synthesis
  • Glycosides / chemistry
  • Ketones / chemical synthesis*
  • Ketones / chemistry
  • Macrolides / chemical synthesis
  • Macrolides / chemistry
  • Molecular Structure
  • Sulfhydryl Compounds / chemistry*

Substances

  • Anti-Bacterial Agents
  • Biological Products
  • Glycosides
  • Ketones
  • Macrolides
  • Sulfhydryl Compounds
  • callipeltoside A
  • lyngbouilloside