Asymmetric bisboranes as bidentate catalysts for carbonyl substrates

Org Lett. 2009 Feb 5;11(3):713-5. doi: 10.1021/ol802793k.

Abstract

A new class of C(2) symmetric bisoxazaborolidinone compounds is described which exhibits bidentate binding to carbonyl substrates. Using the Diels-Alder reaction as a model system, the catalytic activity of these bis-Lewis acids is probed. Reaction rates and selectivities are observed that are higher than the corresponding mono-Lewis acids. This novel system offers a potentially powerful new approach to asymmetric Lewis acid catalysis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boranes / chemical synthesis*
  • Boranes / chemistry
  • Catalysis
  • Heterocyclic Compounds, 1-Ring / chemistry*
  • Ketones / chemistry*
  • Ligands
  • Models, Molecular*
  • Molecular Structure

Substances

  • Boranes
  • Heterocyclic Compounds, 1-Ring
  • Ketones
  • Ligands
  • oxazaborolidinone