Selective C−H or N−H Imidoylative Annulation of 2‐(2‐Isocyanophenyl)‐1 H ‐indoles Leading to Diverse Indole‐fused Scaffolds-Reference-Cited by-同舟云学术

Selective C−H or N−H Imidoylative Annulation of 2‐(2‐Isocyanophenyl)‐1 H ‐indoles Leading to Diverse Indole‐fused Scaffolds

Published:2019-01-29 Issue:6 Volume:361 Page:1414-1418
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Teng Fan¹²,Hu Weiming¹²,Hu Huaanzi¹²,Luo Shuang¹²,Zhu Qiang¹²

Affiliation:

1. State Key Laboratory of Respiratory Disease, Guangzhou Institutes of Biomedicine and HealthChinese Academy of Sciences 190 Kaiyuan Avenue Guangzhou 510530 People's Republic of China

2. University of Chinese Academy of Sciences No. 19(A) Yuquan Road, Shijingshan District Beijing 100049 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201801623

Reference53 articles.

1. For selected reviews see:

2. Palladium-Catalyzed Migratory Insertion of Isocyanides: An Emerging Platform in Cross-Coupling Chemistry

3. Unravelling the labyrinth of palladium-catalysed reactions involving isocyanides

4. Recent advances in isocyanide insertion chemistry

5. To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis

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