An unprecedented Pd-catalyzed, water-promoted sequential oxidative aminocarbonylation-cyclocarbonylation process leading to 2-oxazolidinones

Org Lett. 2007 Aug 16;9(17):3319-22. doi: 10.1021/ol071332c. Epub 2007 Jul 26.

Abstract

An unprecedented, PdI2-catalyzed, sequential oxidative aminocarbonylation-cyclocarbonylation process, leading to 2-oxazolidinone derivatives 3 in good to excellent yields starting from readily available alpha,alpha-disubstituted 2-ynylamines 1 and secondary amines 2, is reported. In the case of an alpha-monosubstituted substrate, the initially formed 2-oxazolidinone derivative underwent shift of the double bond to give a 3H-oxazol-2-one derivative in excellent isolated yield.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Oxazolidinones / chemical synthesis*
  • Oxidation-Reduction
  • Palladium / chemistry
  • Water / chemistry

Substances

  • Oxazolidinones
  • Water
  • Palladium