An Efficient Route to 3-Aryl-Substituted Quinolin-2-one and 1,8-Naphthyridin-2-one Derivatives of Pharmaceutical Interest
Author:
Affiliation:
1. National Technical University of Athens, School of Chemical Engineering, Laboratory of Organic Chemistry, Zografou Campus, Athens 15773, Greece ojmark@orfeas.chemeng.ntua.gr
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0340051
Reference17 articles.
1. 3'-(Arylmethyl)- and 3'-(Aryloxy)-3-phenyl-4-hydroxyquinolin- 2(1H)-ones: Orally Active Antagonists of the Glycine Site on the NMDA Receptor
2. 4-Substituted-3-phenylquinolin-2(1H)-ones: Acidic and Nonacidic Glycine Site N-Methyl-d-aspartate Antagonists with in Vivo Activity
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