Total Synthesis of Spiro[cyclohexane‐2‐indoline] Alkaloids: A Regio‐ and Diastereoselective Spirocyclization Approach-Reference-Cited by-同舟云学术

Total Synthesis of Spiro[cyclohexane‐2‐indoline] Alkaloids: A Regio‐ and Diastereoselective Spirocyclization Approach

Published:2022-11-10 Issue:49 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Chen Lu¹²,Xie Kejing¹,Zhang Jingyang¹,Zu Liansuo¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology (Ministry of Education) Beijing Advanced Innovation Center for Structural Biology & Frontier Research Center for Biological Structure Tsinghua University Beijing 100084 China

2. Key Laboratory of Biopesticide and Chemical Biology (Ministry of education) College of Plant Protection Fujian Agriculture and Forestry University Fuzhou Fujian 350002 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202212042

Reference47 articles.

2. Lapidilectine A and lapidilectine B, two new alkaloids from Kopsia lapidilecta

3. Alkaloids of Kopsia lapidilecta

4. Lundurines A–D, cytotoxic indole alkaloids incorporating a cyclopropyl moiety from Kopsia tenuis and revision of the structures of tenuisines A–C

5. Grandilodines A−C, Biologically Active Indole Alkaloids from Kopsia grandifolia

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