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Phosphine-Catalyzed [4+3] Annulation Reaction of Indole Derivatives with MBH Carbonates:A Facile Access to Indole-1,2-fused 1,4-Diazepinones and Azepines

[4+3] Annulation Reaction of Indole Derivatives with MBH Carbonates: A Facile Access to Indole-1,2-fused 1,4-Diazepinones and Azepines

作     者:Yannan Zhu Haoran Jiang Yi-Ning Wang Yannan Zhu;Haoran Jiang;Yi-Ning Wang

作者机构:Faculty of Chemistry and Chemical EngineeringYancheng Institute of TechnologyYanchengJiangsu224051 China 

出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))

年 卷 期:2024年第42卷第3期

页      面:271-275页

核心收录:

学科分类:07[理学] 070303[理学-有机化学] 0703[理学-化学] 

基  金:the financial support from the funding for school-level research projects of Yancheng Institute of Technology(No.XJR2022019 XJ201719). 

主  题:Phosphine catalysis [4+3]Annulation Indole derivatives Nitrogen heterocycles Organocatalysis 

摘      要: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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