Ketonization of incarcerated acetophenone enol

J Am Chem Soc. 2003 Aug 13;125(32):9558-9. doi: 10.1021/ja030094n.

Abstract

A free-standing simple enol has been generated inside a carceplex. Rates of ketonization under various conditions were determined; ketonization is extremely slow as compared to the rate in solution. Complexed water is required, and the mechanism proceeds via formation of an enolate followed by protonation at carbon by the same molecule of water that removed the proton from the enol. Acid or base retards ketonization by removing water from the cavity.

Publication types

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

MeSH terms

  • Acetophenones / chemistry*
  • Ethylenes / chemistry
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Photolysis

Substances

  • Acetophenones
  • Ethylenes