McLeod David A, Thøgersen Mathias Kirk, Barløse Casper Larsen, Skipper Mette Louise, Obregón Erlaitz Basabe, Jørgensen Karl Anker
Department of Chemistry, Aarhus University, 8000, Aarhus C, Denmark.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202206096. doi: 10.1002/anie.202206096. Epub 2022 May 31.
A novel enantioselective (8+3) cycloaddition between donor-acceptor cyclopropanes and heptafulvenoids catalysed by a chiral bifunctional Brønsted base is described. Importantly, the reaction, which leverages an anionic activation strategy, is divergent from prototypical Lewis-acid activation protocols. A series of cyclopropylketones react with tropones affording the desired (8+3) cycloadducts in high yield and enantiomeric excess. For barbiturate substituted heptafulvenes, the (8+3) cycloaddition with cyclopropylketones proceeds in good yield, excellent diastereoselectivity and high enantiomeric excess. The experimental work is supported by DFT calculations, which indicate that the bifunctional organocatalyst activates both the donor-acceptor cyclopropane and tropone; the reaction proceeds in a step-wise manner with the ring-closure being the stereodetermining step.
本文描述了一种由手性双功能布朗斯特碱催化的给体-受体环丙烷与庚富烯类化合物之间新型的对映选择性(8+3)环加成反应。重要的是,该反应采用阴离子活化策略,与典型的路易斯酸活化方案不同。一系列环丙基酮与环庚三烯反应,以高收率和对映体过量得到所需的(8+3)环加成产物。对于巴比妥酸取代的庚富烯,与环丙基酮的(8+3)环加成反应收率良好,非对映选择性优异,对映体过量高。密度泛函理论(DFT)计算支持了实验工作,结果表明双功能有机催化剂同时活化给体-受体环丙烷和环庚三烯;反应以逐步方式进行,闭环是立体决定性步骤。