Diels-Alder approach to biaryls: elucidation of competing tandem [2+2] cycloaddition/[1,3] sigmatropic shift pathway

J Org Chem. 2008 Sep 19;73(18):7305-9. doi: 10.1021/jo801245a. Epub 2008 Aug 22.

Abstract

Reaction of 2-halo-6-nitrophenylacetylene with an electron deficient diene gives rise to a [4+2] cycloaddition/cycloreversion biaryl product and a bicyclo[4.2.0]octadiene resulting from a competing [2+2] cycloaddition pathway. The cyclobutene can be opened to give a mixture of cyclooctatriene and biaryl in varying amounts depending on heat and light exposure. The conversion of the cyclobutene into biaryl occurs through a [1,3] sigmatropic carbon shift followed by [4+2] cycloextrusion of ethylene gas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biphenyl Compounds / chemical synthesis*
  • Biphenyl Compounds / chemistry
  • Cyclization
  • Cyclobutanes / chemistry
  • Molecular Structure
  • Stereoisomerism

Substances

  • Biphenyl Compounds
  • Cyclobutanes