Access to Polycyclic Indol(en)ines via Base‐Catalyzed Intramolecular Dearomatizing 3‐Alkenylation of Alkynyl Indoles-Reference-Cited by-同舟云学术

Access to Polycyclic Indol(en)ines via Base‐Catalyzed Intramolecular Dearomatizing 3‐Alkenylation of Alkynyl Indoles

Published:2021-06-25 Issue:8 Volume:39 Page:2207-2212
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Lu Lin¹,Zheng Zuoliang²,Yang Yongjie¹,Liu Bo²³,Yin Biaolin¹

Affiliation:

1. Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering South China University of Technology Guangzhou Guangdong 510640 China

2. The Second Clinical Medical College, and Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome Guangzhou University of Chinese Medicine Guangzhou Guangdong 510006 China

3. Guangzhou Key Laboratory of Chirality Research on Active Components of Traditional Chinese Medicine Guangzhou Guangdong 510006 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202100164

Reference56 articles.

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2. Non-monoterpenoid azepinoindole alkaloids

3. Tryptophol and derivatives: natural occurrence and applications to the synthesis of bioactive compounds

4. For reviews on dearomatization reactions see: (a) Zhang D.; Song H.; Qin Y. Total Synthesis of Indoline Alkaloids: A Cyclopropanation Strategy.Acc. Chem. Res.2011 44 447–457;

5. Catalytic Asymmetric Dearomatization Reactions

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