Three-Component Synthesis of Isoquinolone Derivatives via Rh(III)-Catalyzed C–H Activation and Tandem Annulation
Author:
Affiliation:
1. School of Chemistry and Chemical Engineering/Institute of Clean Energy and Materials/Guangzhou Key Laboratory for Clean Energy and Materials, Guangzhou University, Guangzhou 510006, P. R. China
Funder
Guangdong Science and Technology Department
National Natural Science Foundation of China
Guangzhou City
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02181
Reference53 articles.
1. Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (2)
2. Design and Synthesis of Indenoisoquinolines Targeting Topoisomerase I and Other Biological Macromolecules for Cancer Chemotherapy
3. New Strategies in the Discovery of Novel Non-Camptothecin Topoisomerase I Inhibitors
4. Indenoisoquinoline Topoisomerase Inhibitors Strongly Bind and Stabilize the MYC Promoter G-Quadruplex and Downregulate MYC
5. Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C−H/N−H Activation
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