Biomimetic total synthesis of cruentaren A via aromatization of diketodioxinones

J Org Chem. 2012 Apr 6;77(7):3060-70. doi: 10.1021/jo300225z. Epub 2012 Mar 15.

Abstract

The total synthesis of cruentaren A, a biologically active resorcylate natural product, is reported. The aromatic unit was constructed via late-stage cyclization and aromatization from a diketodioxinone intermediate and macrocyclization using Fürstner ring-closing alkyne metathesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetics
  • Cyclization
  • Ketones / chemistry*
  • Macrolides / chemical synthesis*
  • Macrolides / chemistry*
  • Molecular Structure

Substances

  • Ketones
  • Macrolides
  • cruentaren A