Symmetrical bisquinolones via metal-catalyzed cross-coupling and homocoupling reactions

J Org Chem. 2006 Feb 17;71(4):1707-10. doi: 10.1021/jo052283p.

Abstract

Functionalized 4,4'-bisquinolones can be efficiently synthesized by microwave-assisted palladium(0)-catalyzed one-pot borylation/Suzuki cross-coupling reactions or via nickel(0)-mediated homocouplings of 4-chloroquinolin-2(1H)-one precursors. Both methods are also applicable to other types of symmetrical biaryls.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Microwaves
  • Nickel
  • Palladium
  • Quinolones / chemical synthesis*

Substances

  • Quinolones
  • Palladium
  • Nickel