Selectfluor-Mediated Regioselective C-3 Alkoxylation, Amination, Sulfenylation, and Selenylation of Quinoxalin-2(1H)-ones
Author:
Affiliation:
1. Department of Chemistry, Birla Institute of Technology and Science, Pilani, Pilani Campus, Rajasthan 333031, India
2. Department of Chemistry, Birla Institute of Technology and Science, Pilani, Hyderabad Campus, Telangana 500078, India
Funder
Council of Scientific and Industrial Research
Science and Engineering Research Board
Department of Science and Technology, Ministry of Science and Technology
Birla Institute of Technology and Science, Pilani
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02756
Reference42 articles.
1. Chemistry, Biological Properties and SAR Analysis of Quinoxalinones
2. Design and Synthesis of Potent and Multifunctional Aldose Reductase Inhibitors Based on Quinoxalinones
3. Design, synthesis and molecular docking study of novel quinoxalin-2(1H)-ones as anti-tumor active agents with inhibition of tyrosine kinase receptor and studying their cyclooxygenase-2 activity
4. Quinoxalinone as a Privileged Platform in Drug Development
5. A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells
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1. Iron‐Catalyzed Direct C3−H Trifluoromethylthiolation of Quinoxalin‐2(1H)‐ones;Advanced Synthesis & Catalysis;2023-12-20
2. Three‐Component Reactions of Quinoxalin‐2(1H)‐ones: Recent Advances;European Journal of Organic Chemistry;2023-09-27
3. Metal-Free Addition of Alkyl Bromides to Access 3,3-Disubstituted Quinoxalinones Enabled by Visible-Light Photoredox Catalysis;The Journal of Organic Chemistry;2023-08-09
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