Biomimetic total syntheses of linderaspirone A and bi-linderone and revisions of their biosynthetic pathways

Org Lett. 2011 May 6;13(9):2192-5. doi: 10.1021/ol200418e. Epub 2011 Mar 29.

Abstract

Simple exposure to sunlight is sufficient for triggering photochemical [2 + 2] cycloaddition-Cope or radical rearrangement cascades in the naturally occurring methyl linderone, leading to efficient biomimetic total syntheses of linderaspirone A and bi-linderone, two recently discovered bioactive spirocyclopentenedione natural products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetic Materials / chemical synthesis*
  • Dimerization
  • Lactones / chemical synthesis*
  • Models, Molecular
  • Molecular Structure
  • Spiro Compounds / chemical synthesis*

Substances

  • Lactones
  • Spiro Compounds
  • bi-linderone
  • linderaspirone A