Protecting‐Group‐Free Total Synthesis and Biological Investigation of Cabucine Oxindole A †-Reference-Cited by-同舟云学术

Protecting‐Group‐Free Total Synthesis and Biological Investigation of Cabucine Oxindole A †

Published:2020-12-16 Issue:1 Volume:39 Page:137-142
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Xie Shengling¹,Ning Chengqing¹,Yu Qingzhen¹,Hou Jieping¹,Xu Jing¹

Affiliation:

1. Department of Chemistry and Shenzhen Grubbs Institute and Guangdong Provincial Key Laboratory of Catalysis and Shenzhen Key Laboratory of Small Molecule Drug Discovery and Synthesis, Southern University of Science and Technology, Shenzhen Guangdong 518055 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202000460

Reference77 articles.

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3. Natural Product-Derived Spirooxindole Fragments Serve as Privileged Substructures for Discovery of New Anticancer Agents

4. An overview of spirooxindole as a promising scaffold for novel drug discovery

5. For selected recent synthesis see: (a) Shimokawa J.; Harada T.; Yokoshima S.; Fukuyama T. Total synthesis of gelsemoxonine.J. Am. Chem. Soc.2011 133 17634–17637;

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