Total Synthesis and Absolute Configuration of the Guaiane Sesquiterpene Englerin A

Matthieu Willot, Lea Radtke, Daniel Könning, Roland Fröhlich, Viktoria H. Gessner, Carsten Strohmann, Mathias Christmann

Angewandte Chemie International Edition · 2009 · 129 citations · 27 references

Concepts

Abstract

Catnip craze: Nepetalactone, the psychoactive ingredient of catmint, was selected as starting material for the first enantioselective synthesis of englerin A. This cytotoxic guaiane sesquiterpene is a highly selective inhibitor (1–87 nM) of several renal cancer cell lines. The absolute configuration of this natural product was determined by total synthesis.

References

27