Kato Hiroki, Musha Itsuki, Komatsuda Masaaki, Muto Kei, Yamaguchi Junichiro
Department of Applied Chemistry, Waseda University 3-4-1, Ohkubo, Shinjuku Tokyo 169-8555 Japan
Waseda Institute for Advanced Study, Waseda University Shinjuku Tokyo 169-8050 Japan
Chem Sci. 2020 Jul 29;11(33):8779-8784. doi: 10.1039/d0sc02881a.
A Pd-catalyzed dearomative three-component C-C bond formation of bromoarenes with diazo compounds and malonates was developed. Various bromoarenes ranging from benzenoids to azines and heteroles were transformed to the corresponding substituted alicyclic molecules. The key to this reaction is the generation of a benzyl-palladium intermediate, which reacts with malonates to form a Pd--enolate species. Strikingly, the present method enabled rapid access to multi-substituted alicycles through subsequent elaboration of dearomatized products.
开发了一种钯催化的溴代芳烃与重氮化合物和丙二酸酯的脱芳构化三组分C-C键形成反应。从苯类到嗪类和杂环类的各种溴代芳烃都被转化为相应的取代脂环族分子。该反应的关键是生成苄基钯中间体,它与丙二酸酯反应形成钯-烯醇化物物种。引人注目的是,本方法能够通过后续对脱芳构化产物的修饰快速获得多取代脂环。