Regioselective three-component synthesis of 2,3-disubstituted quinolines via the enaminone modified Povarov reaction
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering
2. Jiangxi Normal University
3. Nanchang 330022
4. P.R. China
5. Research Center of Analysis and Measurement
6. Zhejiang University of Technology
7. Hangzhou
8. P. R. China
Abstract
The enaminone modified three-component Povarov reactions enable the regioselective synthesis of 2,3-disubstituted quinolines.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Jiangxi Province
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB02411H
Reference94 articles.
1. Recent synthetic developments in a powerful imino Diels–Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids
2. Advances in the Chemistry of Tetrahydroquinolines
3. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction
4. Chiral Brønsted Acid-Catalyzed Enantioselective Three-Component Povarov Reaction
5. Chiral Phosphoric Acid-Catalyzed Enantioselective Three-Component Povarov Reaction Using Enecarbamates as Dienophiles: Highly Diastereo- and Enantioselective Synthesis of Substituted 4-Aminotetrahydroquinolines
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