Synthesis of functionalized vinyl boronates via ruthenium-catalyzed olefin cross-metathesis and subsequent conversion to vinyl halides

J Org Chem. 2003 Jul 25;68(15):6031-4. doi: 10.1021/jo0345345.

Abstract

Functionalized vinyl pinacol boronates suitable for Suzuki cross-coupling reactions are synthesized using ruthenium-catalyzed olefin cross-metathesis of 1-propenyl pinacol boronate and various alkenes, including functionalized and 1,1-disubstituted alkenes. The resultant boronate cross products are stereoselectively transformed into predominantly Z-vinyl bromides and E-vinyl iodides. The vinyl bromides may be synthesized in a two-step, one-pot synthesis from a variety of olefins, resulting in a Z-selective formal vinyl bromide cross-metathesis reaction.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alkenes / chemistry*
  • Anions
  • Boronic Acids / chemical synthesis*
  • Boronic Acids / chemistry
  • Catalysis
  • Indicators and Reagents
  • Models, Molecular
  • Ruthenium*
  • Vinyl Compounds / chemical synthesis*
  • Vinyl Compounds / chemistry

Substances

  • Alkenes
  • Anions
  • Boronic Acids
  • Indicators and Reagents
  • Vinyl Compounds
  • Ruthenium