吲哚试验
废止
化学
合成子
磷化氢
组合化学
催化作用
吲哚生物碱
有机化学
立体化学
药物化学
作者
Yannan Zhu,Haoran Jiang,Yining Wang
标识
DOI:10.1002/cjoc.202300505
摘要
Comprehensive Summary A phosphine‐catalyzed [4+3] annulation between dinucleophilic indole derivatives and Morita−Baylis−Hillman (MBH) carbonates was discovered by using the N1 and N4′/C4′ nucleophilicities of the indole precursors, in which indoles act as four atom synthons. This protocol provides an efficient and facile access to indole‐1,2‐fused 1,4‐diazepinones and azepines in good to high yields in one step, which illustrates potential synthetic utilities in drug discovery.
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