EaStCHEM, School of Chemistry, University of St Andrews, North Haugh, Fife, St AndrewsKY16 9ST, U.K.
GlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, StevenageSG1 2NY, U.K.
J Org Chem. 2022 Nov 18;87(22):15559-15563. doi: 10.1021/acs.joc.2c02099. Epub 2022 Oct 19.
A concise strategy for the total synthesis of several alkaloids is reported. A Suzuki-Miyaura cross-coupling provides access to a 2-vinyl indole that undergoes a Diels-Alder cascade reaction with butyn-2-one to deliver a pyrroloindoline intermediate. This undergoes cascade amidation, reduction, skeletal rearrangement, and intramolecular Michael addition to provide a common intermediate containing the full framework of the alkaloids. The utility of this intermediate is shown in the synthesis of four different natural products.
报告了一种简洁的策略,用于几种生物碱的全合成。Suzuki-Miyaura 交叉偶联提供了一个 2-乙烯基吲哚,它与丁炔-2-酮发生 Diels-Alder 级联反应,生成吡咯并吲哚啉中间体。该中间体经历级联酰胺化、还原、骨架重排和分子内迈克尔加成,提供了一个包含生物碱全骨架的共同中间体。该中间体的用途在四个不同天然产物的合成中得到了展示。