Highly efficient isobutyraldehyde-mediated epoxidation of cyclic alkenes with dioxygen catalyzed by a novel dimeric manganese(II) complex containing an easy-to-prepare flexible carboxamide ligand

Inorg Chem. 2009 Jul 6;48(13):5593-5. doi: 10.1021/ic900334w.

Abstract

Dioxygen epoxidation of cyclic alkenes into their corresponding epoxides was successfully achieved in good yield by using a novel binuclear manganese carboxamide complex as the catalyst and isobutyraldehyde as the cosubstrate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry
  • Alkenes / chemistry*
  • Catalysis
  • Cyclization
  • Epoxy Compounds / chemistry*
  • Manganese / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Oxygen / chemistry*
  • X-Ray Diffraction

Substances

  • Aldehydes
  • Alkenes
  • Epoxy Compounds
  • Manganese
  • isobutyraldehyde
  • Oxygen