Regioselective N-Methylation of 6-Chloroindolo[3,2-c]quinolines and Their Amination Reactivity at the C-6 Position
Author:
Affiliation:
1. Division of Chemistry and Biotechnology, Graduate School of Natural Science and Technology, Okayama University
2. Department of Applied Chemistry, Faculty of Engineering, Okayama University of Science
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20130063
Reference21 articles.
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1. Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro-6H-indolo[3,2-c]quinolin-6-ones as Potent Topoisomerase-I Inhibitors;Journal of Medicinal Chemistry;2021-01-25
2. Methods of synthesis of natural indoloquinolines isolated from Cryptolepis sanguinolenta;Chemistry of Heterocyclic Compounds;2019-10
3. Convenient Synthesis of 11-Substituted 11H -Indolo[3,2-c ]quinolines by Sequential Chemoselective Suzuki Reaction/Double C-N Coupling;European Journal of Organic Chemistry;2017-10-04
4. Synthesis and structure-activity relationships of novel neocryptolepine derivatives;Chemical Research in Chinese Universities;2017-05-11
5. Construction of indoloquinolinones via Pd(II)-catalyzed tandem CC/CN bond formation: application to the total synthesis of isocryptolepine;Tetrahedron Letters;2014-12
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