Department of Chemistry and Pharmaceutical Sciences, Amsterdam Institute of Molecular and Life Sciences (AIMMS), De Boelelaan 1108, 1081 HZ, Amsterdam, The Netherlands.
Angew Chem Int Ed Engl. 2022 Oct 17;61(42):e202210592. doi: 10.1002/anie.202210592. Epub 2022 Sep 12.
We report an intramolecular conjugate addition/Truce-Smiles/E1cb cascade of 2-nitrobenzenesulfonamide-functionalized cyclohexenones as a new entry to the core scaffold of monoterpene indole alkaloids. The method was applied to the asymmetric total synthesis of (-)-limaspermidine, (-)-kopsinilam, and (-)-kopsinine, as well as the framework of the kopsifoline alkaloids, thus highlighting its complementarity to existing approaches involving the use of indole-based starting materials or the interrupted Fischer indole synthesis. Furthermore, we show that the cascade tolerates various substituents on the nitroarene, opening the way to other natural products as well as non-natural analogues.
我们报告了 2-硝基苯磺酰胺功能化环己烯酮的分子内共轭加成/Truce-Smiles/E1cb 级联反应,这是萜类吲哚生物碱核心骨架的新途径。该方法被应用于(-)-limaspermidine、(-)-kopsinilam 和(-)-kopsinine 的不对称全合成,以及 kopsifoline 生物碱的骨架构建,从而突出了其与现有方法的互补性,这些方法涉及使用吲哚基起始原料或中断的 Fischer 吲哚合成。此外,我们表明该级联反应可以容忍硝基芳烃上的各种取代基,为其他天然产物以及非天然类似物开辟了道路。