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

Aniello PalmaMarkus ArtelsmairGuanglu WuXiaoyong LuSteven J BarrowNajib UddinEdina RostaEric MassonOren A Scherman
Published in: Angewandte Chemie (International ed. in English) (2017)
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.
Keyphrases
  • water soluble
  • energy transfer
  • molecular docking
  • molecular dynamics simulations
  • amino acid