超分子化学
合成子
超分子催化
酶
化学
天然产物
人工酶
水溶液
催化作用
基质(水族馆)
组合化学
生物催化
立体化学
有机化学
反应机理
生物
分子
生态学
作者
Aniello Palma,Markus Artelsmair,Guanglu Wu,Xiaoyong Lu,Steven J. Barrow,Najib Uddin,Edina Rosta,Eric Masson,Oren A. Scherman
标识
DOI:10.1002/anie.201706487
摘要
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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