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四丁基碘化胺催化活化烯烃烷氧羰基化反应:合成异喹啉二酮衍生物 被引量:7

Tetrabutylammonium Iodide-Catalyzed Radical Alkoxycarbonylation of Activated Alkenes: Synthesis of Isoquinolinedione Derivatives
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摘要 异喹啉二酮骨架是一种重要的有机合成砌块,广泛存在于生物碱、天然产物和药物中.提供了一种非金属催化构建异喹啉二酮骨架结构的新方法.机理研究表明,该反应经历了一个自由基过程:在四丁基碘化胺催化作用下,肼化合物质子被逐步攫取生成烷氧羰基自由基,随后对活化烯烃进行自由基加成反应,进一步环化形成异喹啉二酮骨架.该方法具有反应条件温和、底物普适性广、环境友好等特点,为合成含异喹啉二酮骨架分子结构提供了一种新途径. The isoquinolinedione skeletons are important building blocks, which have been widely present in plant alkaloids, natural products and pharmaceuticals. In this paper, a novel method to construct isoquinolinedione framework was developed, which can be easily operated under metal-free conditions. In the presence of tetrabutylammonium-iodide catalyst, hydrogen atoms were abstracted step by step from carbazate to generate methoxycarbonyl radical which followed by radical addition/ cyclization reaction leading to isoquinolinedione. The presented methodology will provide new strategies for construct iso- quinolinedione-type products, which has advantages of simple operation, mild reaction conditions, and environmentally be- nign.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2015年第4期875-881,共7页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No.21102130) 浙江省科技创新团队(Nos.2010R50018 2011R50017)资助项目~~
关键词 异喹啉二酮结构 非金属催化 四丁基碘化胺 自由基加成/环化 isoquinolinedione skeleton metal-free tetrabutylammonium-iodide radical addition/cyclization
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  • 1Jaegli, S.; Dufour, J.; Wei, H.; Piou, T.; Duan, X. H.; Vors, J. P.; Neuville, L.; Zhu, J. Org. Lett.2010,12,4498.
  • 2Wei, H.; Piou, T.; Dufour, J.; Neuville, L.; Zhu, J. Org. Lett.2011,13,2244.
  • 3Mu, X.; Wu, T.; Wang, H.; Guo, Y.; Liu, G. J. Am. Chem. Soc.2012,134,878.
  • 4Li, Y. M.; Sun, M.; Wang, H. L.; Tian, Q. P.; Yang, S. D. Angew. Chem., Int. Ed.2013,52,3972.
  • 5Wei, W. T.; Zhou, M. B.; Fan, J. H.; Liu, W.; Song, R. J.; Liu, Y.; Hu, M.; Xie, P.; Li, J. H. Angew. Chem., Int. Ed.2013,52,3638.
  • 6Shen, T.; Yuan, Y.; Song, S.; Jiao, N. Chem. Commun.2014,50,4115.
  • 7Dai, Q.; Yu, J.; Jiang, Y.; Guo, S.; Yang, H.; Cheng, J. Chem. Commun.2014,50,3865.
  • 8Zhou, S. L.; Guo, L. N.; Wang, H.; Duan, X. H. Chem. Eur. J.2013,19,12970.
  • 9Wang, H.; Guo, L. N.; Duan, X. H. Adv. Synth. Catal.2013,355,2222.
  • 10Wang, H.; Guo, L. N.; Duan, X. H. Chem. Commun.2013,49,10370.

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