4.5 Article

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

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2017, Issue 32, Pages 4773-4777

Publisher

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

Keywords

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

Funding

  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]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available