Selective oxygenation of alkynes: a direct approach to diketones and vinyl acetate

Org Biomol Chem. 2014 Dec 28;12(48):9909-13. doi: 10.1039/c4ob01404a.

Abstract

Arylalkynes can be converted into α-diketones with the use of a copper catalyst, and also be transformed into vinyl acetates under metal-free conditions, both in the presence of PhI(OAc)2 as an oxidant at room temperature. A series of substituted α-diketones were prepared in moderate to good yields. A variety of vinyl halides could be regio- and stereo-selectively synthesized under mild conditions, and I, Br and Cl could be all easily embedded into the alkynes.

Publication types

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

MeSH terms

  • Alkynes / chemistry*
  • Crystallography, X-Ray
  • Ketones / chemical synthesis*
  • Ketones / chemistry
  • Models, Molecular
  • Molecular Structure
  • Oxygen / chemistry*
  • Vinyl Compounds / chemical synthesis*
  • Vinyl Compounds / chemistry

Substances

  • Alkynes
  • Ketones
  • Vinyl Compounds
  • vinyl acetate
  • Oxygen