Aryne acyl-alkylation in the general and convergent synthesis of benzannulated macrolactone natural products: an enantioselective synthesis of (-)-curvularin

Org Lett. 2010 Apr 2;12(7):1612-4. doi: 10.1021/ol100335y.

Abstract

A general approach for the synthesis of benzannulated macrolactone natural products utilizing an aryne acyl-alkylation reaction is described. Toward this end, the total syntheses of the natural products (-)-curvularin, curvulin, and (-)-diplodialide C are reported. Furthermore, the aryne insertion technology has enabled the rapid conversion of simple diplodialide natural products to curvularin, thereby connecting these two biosynthetically distinct classes of compounds via synthetic methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Biological Factors / chemical synthesis*
  • Biological Factors / chemistry
  • Macromolecular Substances / chemical synthesis
  • Macromolecular Substances / chemistry
  • Molecular Structure
  • Stereoisomerism
  • Zearalenone / analogs & derivatives*
  • Zearalenone / chemical synthesis
  • Zearalenone / chemistry

Substances

  • Biological Factors
  • Macromolecular Substances
  • Zearalenone
  • curvularin