Total synthesis of asterredione

J Org Chem. 2014 Mar 7;79(5):2111-4. doi: 10.1021/jo4028177. Epub 2014 Feb 17.

Abstract

The first total synthesis of asterredione was efficiently accomplished over five linear steps and in 21.5% overall yield. As the crucial step, the 2-quaternary 1,3-cyclopentenedione skeleton of asterredione was readily achieved using the Darzens/ring-expansion strategy developed in our laboratory. The structure of synthesized asterredione was fully confirmed by X-ray crystallography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Cyclopentanes / chemical synthesis
  • Cyclopentanes / chemistry*
  • Indoles / chemical synthesis*
  • Indoles / chemistry
  • Molecular Structure
  • Stereoisomerism

Substances

  • Cyclopentanes
  • Indoles
  • asterredione