Tunable synthesis of quinolinone-fused isoquinolines through sequential one-pot nucleophilic addition and palladium-catalyzed intramolecular C–H alkenylation
Author:
Affiliation:
1. Department of Chemistry and Chemical Engineering
2. College of Science
3. P. R. China
4. Material Science and Engineering College
5. Northeast Forestry University
Abstract
An efficient sequential one-pot synthesis of N-fused heterocycles based on 4-quinolinone and isoquinoline scaffolds of biological interest has been developed.
Funder
Natural Science Foundation of Heilongjiang Province
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB02437E
Reference36 articles.
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2. Bacterial Topoisomerase Inhibitors: Quinolone and Pyridone Antibacterial Agents
3. Origins of the Quinolone Class of Antibacterials: An Expanded “Discovery Story”
4. The chemistry and biological activity of heterocycle-fused quinolinone derivatives: A review
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