Asymmetric Cycloaddition of <i>N</i>-2,2,2-Trifluoroethylisatin Ketimines and Unsymmetrical Dicarbonyl-Activated Alkenes: Construction of 5′-Trifluoromethylated 3,2′-Pyrrolidinyl Spirooxindoles with Three Carbonyl Groups-Reference-Cited by-同舟云学术

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Asymmetric Cycloaddition of N-2,2,2-Trifluoroethylisatin Ketimines and Unsymmetrical Dicarbonyl-Activated Alkenes: Construction of 5′-Trifluoromethylated 3,2′-Pyrrolidinyl Spirooxindoles with Three Carbonyl Groups

Published:2024-08-28 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

He Jin-Zhi¹,Zhu Bao-Lei¹,Huang Zhen-Hui¹,Liang Jin-Ping¹,Zhang Zhen-Wei¹,Chen Qing²,Lin Ning¹^ORCID

Affiliation:

1. College of Pharmacy, Guangxi Zhuang Yao Medicine Center of Engineering and Technology, Guangxi University of Chinese Medicine, Nanning 530200, P. R. China

2. Guangxi Scientific Research Center of Traditional Chinese Medicine, Guangxi Zhuang Yao Medicine Center of Engineering and Technology, Guangxi University of Chinese Medicine, Nanning, 530200, P. R. China

Funder

Natural Science Foundation of Guangxi Zhuang Autonomous Region

Education Department of Guangxi Zhuang Autonomous Region

Guangxi University of Chinese Medicine

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00805

Reference36 articles.

1. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

2. Natürliche Pyrrolidinylspirooxindole als Vorlagen für die Entwicklung medizinischer Wirkstoffe

3. Spirooxindoles: Promising scaffolds for anticancer agents

4. Therapeutic Potential of Spirooxindoles as Antiviral Agents

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