A novel palladium-catalyzed dicarbonylation process leading to coumarins

J Org Chem. 2008 Jan 18;73(2):756-9. doi: 10.1021/jo702243m. Epub 2007 Dec 14.

Abstract

A novel approach to coumarin derivatives has been developed starting from readily available 2-(1-hydroxyprop-2-ynyl)phenols, based on an unprecedented palladium-catalyzed dicarbonylation process. Reactions were carried out in the presence of catalytic amounts of PdI2 in conjunction with an excess of KI in MeOH as the solvent at room temperature and under 90 atm of CO to give 3-[(methoxycarbonyl)methyl]coumarins in good to high isolated yields (62-87%).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbon Monoxide / chemistry
  • Catalysis
  • Coumarins / chemical synthesis*
  • Coumarins / chemistry
  • Cyclization
  • Molecular Structure
  • Palladium / chemistry*
  • Phenols / chemistry
  • Stereoisomerism

Substances

  • Coumarins
  • Phenols
  • Palladium
  • Carbon Monoxide