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Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions.
Palma, Aniello; Artelsmair, Markus; Wu, Guanglu; Lu, Xiaoyong; Barrow, Steven J; Uddin, Najib; Rosta, Edina; Masson, Eric; Scherman, Oren A.
Afiliação
  • Palma A; Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
  • Artelsmair M; Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
  • Wu G; Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
  • Lu X; Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio, 45701, USA.
  • Barrow SJ; Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
  • Uddin N; Department of Chemistry, King's College London, London, SE1 1DB, UK.
  • Rosta E; Department of Chemistry, King's College London, London, SE1 1DB, UK.
  • Masson E; Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio, 45701, USA.
  • Scherman OA; Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Angew Chem Int Ed Engl ; 56(49): 15688-15692, 2017 12 04.
Article em En | MEDLINE | ID: mdl-29048713
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidrocarbonetos Aromáticos com Pontes / Imidazóis Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidrocarbonetos Aromáticos com Pontes / Imidazóis Idioma: En Ano de publicação: 2017 Tipo de documento: Article