An efficient approach to functionalized benzo[a]xanthones through reactions of 2-methyl-3-(1-alkynyl)chromones with electron-deficient chromone-fused dienes

Org Lett. 2010 Sep 3;12(17):3848-51. doi: 10.1021/ol101496w.

Abstract

An efficient tandem process was developed to synthesize diversified benzo[a]xanthones from 2-methyl-3-(1-alkynyl)chromones with electron-deficient chromone-fused dienes. This unusual reaction, involving multiple steps and not requiring the use of transition metal catalysts or an inert atmosphere, results in the formation of three new C-C bonds and one C-O bond.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Catalysis
  • Chromones / chemistry*
  • Combinatorial Chemistry Techniques
  • Molecular Structure
  • Xanthones / chemical synthesis*
  • Xanthones / chemistry

Substances

  • Alkynes
  • Chromones
  • Xanthones