Divergent Syntheses of Carbazole Alkaloids Clausenapin, Indizoline, Claulansine M, and Clausenaline D

J Org Chem. 2016 May 20;81(10):4310-5. doi: 10.1021/acs.joc.6b00729. Epub 2016 May 5.

Abstract

We described the first total syntheses of clausenapin, indizoline, claulansine M, and a novel synthetic route to clausenaline D via divergent method. Key steps involved TFAA-mediated intramolecular acylation to construct the carbazole core and subsequent Claisen rearrangement to generate key intermediates for further elaboration to target molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Alkaloids / chemical synthesis*
  • Carbazoles / chemical synthesis*
  • Indicators and Reagents
  • Indole Alkaloids
  • Magnetic Resonance Spectroscopy
  • Stereoisomerism

Substances

  • Alkaloids
  • Carbazoles
  • Indicators and Reagents
  • Indole Alkaloids
  • clausenaline D