Rh(iii)-Catalyzed three-component cascade annulation to produce the N-oxopropyl chain of isoquinolone derivatives
Author:
Affiliation:
1. Key Laboratory of Drug Targeting and Drug Delivery System of Ministry of Education
2. West China School of Pharmacy
3. Sichuan University
4. Chengdu 610041
5. China
Abstract
Developing powerful methods to introduce versatile functional groups at the N-substituents of isoquinolone scaffolds is still a great challenge.
Funder
Higher Education Discipline Innovation Project
Fundamental Research Funds for the Central Universities
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02389B
Reference74 articles.
1. A Systematic Study of Nitrated Indenoisoquinolines Reveals a Potent Topoisomerase I Inhibitor
2. Structures of Three Classes of Anticancer Agents Bound to the Human Topoisomerase I−DNA Covalent Complex
3. A novel norindenoisoquinoline structure reveals a common interfacial inhibitor paradigm for ternary trapping of the topoisomerase I-DNA covalent complex
4. Isolation and Structure of Ruprechstyril from Ruprechtia tangarana†,1
5. Lauraceae alkaloids
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1. Green Synthesis of 3,4‐Unsubstituted Isoquinolones through Rhodium(III)‐Catalyzed C−H Activation and Annulation in Ethanol;European Journal of Organic Chemistry;2023-10-24
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