Total synthesis of laetevirenol A

J Org Chem. 2012 Oct 5;77(19):8762-7. doi: 10.1021/jo301345a. Epub 2012 Sep 17.

Abstract

The first complete synthesis of laetevirenol A was performed in nine steps via intramolecular Friedel-Crafts alkylation in a trans-selective manner. The key phenanthrene intermediate was synthesized by a one-pot Suzuki-Miyaura coupling and an aldol condensation cascade reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Catalysis
  • Molecular Structure
  • Phenanthrenes / chemical synthesis*
  • Phenanthrenes / chemistry*
  • Stereoisomerism

Substances

  • Phenanthrenes
  • laetevirenol A
  • phenanthrene