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化学学报
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化学学报 ›› 2013, Vol. 71 ›› Issue (03): 295-298.DOI: 10.6023/A13010018 上一篇    下一篇

研究亮点

中断的Fisher吲哚合成法及其在生物碱合成中的应用

李森a,b, 韩静a, 李昂b   

  1. a 沈阳药科大学制药工程学院 沈阳 110016;
    b 中国科学院上海有机化学研究所生命有机化学国家重点实验室 上海 200032
  • 投稿日期:2013-01-05 发布日期:2013-01-25
  • 通讯作者: 韩静,李昂 E-mail:hj-8080@163.com,ali@sioc.ac.cn
  • 基金资助:

    项目受科技部973计划(No.2013CB836900)、国家自然科学基金(Nos.21172235,21222202,21290180)和上海市浦江人才计划(No.12PJ1410800)和中国科学院资助.

Interrupted Fisher Indole Synthesis and Its Applications to Alkaloid Synthesis

Li Senaa,b, Han Jinga, Li Angb   

  1. a School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016;
    b State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032
  • Received:2013-01-05 Published:2013-01-25
  • Supported by:

    Project supported by the National Basic Research Program (973 Program) of China (No. 2013CB836900), the Natural Science Foundation of China (Nos.21172235, 21222202, and 21290180), Shanghai Pujiang Plan (No. 12PJ1410800) and the Chinese Academy of Sciences.

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被引次数

13 | 4

Fisher吲哚合成是有机合成中的一个重要方法. 近年来, Garg和梁广鑫课题组发展了中断的Fisher吲哚合成法,并将其用于一系列天然产物及类天然产物化合物的合成中. 我们就他们在该领域的工作作一亮点评述.

关键词: Fisher吲哚合成法, [3,3]-sigmatropic重排, 铜催化C—N键形成反应, aspidophylline A, 全合成

Fisher indole synthesis is an important method in organic synthesis. Recently, Garg and Liang developed interrupted Fisher indole synthesis and applied it in the synthesis of a series of natural products and natural product-like compounds. Here we highlight their recent progress under this topic.

Key words: Fisher indole synthesis, [3,3]-sigmatropic rearrangement, Cu-catalyzed C—N bond formation, aspidophylline A, total synthesis