Catalysis with Supramolecular Carbon-Bonding Interactions

被引:15
|
作者
Wang, Wei [1 ]
Li, Xinxin [1 ]
Zhou, Pan-Pan [3 ]
Wang, Yao [1 ,2 ]
机构
[1] Shandong Univ, Minist Educ, Key Lab Colloid & Interface Chem, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[2] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
[3] Lanzhou Univ, Coll Chem & Chem Engn, Key Lab Adv Catalysis Gansu Prov, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon-bonding; catalysts; noncovalent interactions; supramolecular catalysis; terpene cyclization; REACTION PATHS;
D O I
10.1002/anie.202108973
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we describe a new catalysis platform, supramolecular carbon-bonding catalysis, which exploits the highly directional weak interactions between carbon centers of catalysts and electron donors to drive chemical reactions. To demonstrate this catalysis approach, we discovered a class of cyclopropane derivatives incorporated with carbonyl, ester and cyano groups as catalysts which showed general catalysis capability in different types of benchmark reactions. Among these typical examples, a challenging tail-to-head terpene cyclization can be achieved by supramolecular carbon-bonding catalysis. The co-crystal structures of catalyst and electron donors, comparison experiments, and titrations support a catalysis mode of carbon-bonding activation of Lewis basic reactants.
引用
收藏
页码:22717 / 22721
页数:5
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