Melville Laboratory for Polymer Synthesis Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio, 45701, USA.
Angew Chem Int Ed Engl. 2017 Dec 4;56(49):15688-15692. doi: 10.1002/anie.201706487. Epub 2017 Nov 3.
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.
使用超分子构建体(人工酶)模拟天然酶的活性是一个活跃的科学研究领域。在此,我们证明了葫芦[7]脲(CB[7])可以在仿生条件下催化许多取代的和无反应性的 N-烯丙基-2-糠基胺的 Diels-Alder 反应,而无需保护基团,在以前未报道的温和条件下生成强大的合成子。CB[7]将底物重排成高反应性构象,并将其与水相环境隔离,从而模拟天然 Diels-Alderase 的作用模式。这些发现可以直接应用于天然 Diels-Alderase 酶中观察到的产物抑制现象,并为开发新型基于超分子的绿色催化剂铺平道路。