Université de Nantes, CNRS, CEISAM UMR 6230, F-44000 Nantes, France.
J Org Chem. 2021 Dec 17;86(24):18192-18203. doi: 10.1021/acs.joc.1c02459. Epub 2021 Dec 1.
The discovery of a multiple-bond-forming process merging the singlet oxygen-mediated dearomatization of 3,4-disubstitued phenols and diastereo- and regioselective epoxidation is described. This one-pot strategy using a transition metal-free multicatalytic system comprised of rose bengal and cesium carbonate allowed the efficient formation of functionalized epoxyquinol products under mild conditions. Mechanistic investigations have been performed to shed the light on the key species involved in this transformation.
描述了一种多键形成过程的发现,该过程结合了单重态氧介导的 3,4-二取代苯酚去芳构化以及非对映选择性和区域选择性环氧化。这种一锅法策略使用了由孟加拉玫瑰红和碳酸铯组成的无过渡金属多催化体系,允许在温和条件下高效形成功能化的环氧醌产物。进行了机理研究,以阐明这种转化中涉及的关键物种。