Tunable synthesis of quinolinone-fused isoquinolines through sequential one-pot nucleophilic addition and palladium-catalyzed intramolecular C–H alkenylation

Author:

Li Xue12345,Bian Yunyun123,Chen Xin12345,Zhang Hang123,Wang Wei123,Ren Sida123,Yang Xuechen123,Lu Chang123,Chen Chunxia12345,Peng Jinsong123ORCID

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

Reference36 articles.

1. A. F. Pozharskii , A. T.Soldatenkov and A. R.Katritzky , Heterocycles and Health , in Heterocycles in Life and Society , John Wiley , Chichester, UK , 1997 , pp. 135–164

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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