Conjugate Addition Routes to 2‐Alkyl‐2,3‐dihydroquinolin‐4(1 H )‐ones and 2‐Alkyl‐4‐hydroxy‐1,2‐dihydroquinoline‐3‐carboxylates
Author:
Affiliation:
1. GSK Carbon Neutral Laboratories for Sustainable Chemistry University of Nottingham Jubilee Campus NG7 2TU Nottingham United Kingdom
2. Key Organics Ltd Highfield Road Industrial Estate PL32 9RA Camelford Cornwall United Kingdom
Funder
Engineering and Physical Sciences Research Council
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.201901036
Reference29 articles.
1. Origins of the Quinolone Class of Antibacterials: An Expanded “Discovery Story”
2. Synthesis and Functionalization of 4-Quinolones - A Progressing Story
3. Structure–functionality relationship and pharmacological profiles of Pseudomonas aeruginosa alkylquinolone quorum sensing modulators
4. First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist
5. 1-(Arylsulfonyl)-2,3-dihydro-1H-quinolin-4-one derivatives as 5-HT6 serotonin receptor ligands
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1. N-Adamantyl-1-alkyl-4-oxo-1,4-dihydroquinoline-3-carboxamide Derivatives as Fluorescent Probes to Detect Microglia Activation through the Imaging of Cannabinoid Receptor Subtype 2 (CB2R);Journal of Medicinal Chemistry;2024-06-27
2. In SilicoStudy of Thiourea Derivatives as Potential Epidermal Growth Factor Receptor Inhibitors;Journal of Computational Biophysics and Chemistry;2023-03-02
3. Cu(I)-Catalyzed Alkynylation of Quinolones;Organic Letters;2022-01-31
4. Recent Developments in the Synthetic Strategies of 4‐Quinolones and Its Derivatives;ChemistrySelect;2020-11-30
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