Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions

Angew Chem Int Ed Engl. 2017 Dec 4;56(49):15688-15692. doi: 10.1002/anie.201706487. Epub 2017 Nov 3.

Abstract

The ability to mimic the activity of natural enzymes using supramolecular constructs (artificial enzymes) is a vibrant scientific research field. Herein, we demonstrate that cucurbit[7]uril (CB[7]) can catalyse Diels-Alder reactions for a number of substituted and unreactive N-allyl-2-furfurylamines under biomimetic conditions, without the need for protecting groups, yielding powerful synthons in previously unreported mild conditions. CB[7] rearranges the substrate in a highly reactive conformation and shields it from the aqueous environment, thereby mimicking the mode of action of a natural Diels-Alderase. These findings can be directly applied to the phenomenon of product inhibition observed in natural Diels-Alderase enzymes, and pave the way toward the development of novel, supramolecular-based green catalysts.

Keywords: Diels-Alder reactions; biomimetic catalysts; cucurbit[7]uril; enzyme mimics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bridged-Ring Compounds / chemistry*
  • Catalysis
  • Cycloaddition Reaction
  • Imidazoles / chemistry*
  • Macromolecular Substances / chemistry
  • Molecular Structure
  • Thermodynamics

Substances

  • Bridged-Ring Compounds
  • Imidazoles
  • Macromolecular Substances
  • cucurbit(7)uril