4.5 Article

Iodine-Catalyzed Azidation/Cyclization Cascade Approach to 3a-Azidofuroindolines and -pyrroloindolines under Mild Conditions

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2017, 期 32, 页码 4773-4777

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201700618

关键词

Iodine-mediated reactions; Synthetic methods; Iodine; Nitrogen heterocycles; Domino reactions; Fused-ring systems

资金

  1. National Natural Science Foundation of China (NSFC) [21562052, 81573294, 81373285]
  2. Major Project for the Innovation of Industry and Research of Guangzhou City [201508020128]
  3. Guizhou Provincial Department of Science and Technology [LH[2014]7554]

向作者/读者索取更多资源

An efficient and practical approach to 3a-azidofuroindolines and -pyrroloindolines involving an iodine-catalyzed azidation/cyclization cascade of tryptophols and tryptamines with NaN3 was developed. Further transformation of the C3-azidated product provided a key intermediate for the total synthesis of psychotriasine.

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