Convenient Synthesis of <scp>Thioester‐Substituted</scp> Oxindoles by <scp>Palladium‐Catalyzed</scp> Thiocarbonylative Cyclization with Sulfonyl Chlorides as the Sulfur Source-Reference-Cited by-同舟云学术

Convenient Synthesis of Thioester‐Substituted Oxindoles by Palladium‐Catalyzed Thiocarbonylative Cyclization with Sulfonyl Chlorides as the Sulfur Source

Published:2022-12-10 Issue:2 Volume:41 Page:188-192
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Xu Ren‐Rui¹,Fang Xiuyu¹,Qi Xinxin¹,Wu Xiao‐Feng²³

Affiliation:

1. Department of Chemistry, Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, Zhejiang Sci‐Tech University Hangzhou Zhejiang 310018 China

2. Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian Liaoning 116023 China

3. Leibniz‐Institut für Katalyse e.V., Albert‐Einstein‐Straße 29a Rostock 18059 Germany

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202200530

Reference59 articles.

1. Chandra Sekhar;Khetmalis Y. M.;K. V. G. Oxindole and its derivatives: A review on recent progress in biological activities. Biomed. Pharmacother.,2021

2. Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances

3. Review of synthesis and various biological activities of spiro heterocyclic compounds comprising oxindole and pyrrolidine moities

4. Oxindole: A chemical prism carrying plethora of therapeutic benefits

5. Therapeutic Potential of Spirooxindoles as Antiviral Agents

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