Acid-Promoted Direct C–H Carbamoylation at the C-3 Position of Quinoxalin-2(1H)-ones with Isocyanide in Water
Author:
Affiliation:
1. College of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, China
Funder
Chongqing Science and Technology Commission
Chongqing Municipal Education Commission
Chongqing University of Arts and Sciences
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c06946
Reference48 articles.
1. Design and Synthesis of Potent and Multifunctional Aldose Reductase Inhibitors Based on Quinoxalinones
2. Design and syntheses of some new quinoxaline derivatives containing pyrazoline residue as potential antimicrobial agents
3. Quinoxaline, its derivatives and applications: A State of the Art review
4. Advances in the Chemistry of Quinoxalinone Derivatives
5. Functionalized quinoxalinones as privileged structures with broad-ranging pharmacological activities
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1. Visible‐Light Induced C‐3 Carbamoylation of Quinoxalinones Assisted by EDA Complex;Advanced Synthesis & Catalysis;2024-07-23
2. Mn-Mediated Direct Regioselective C–H Trifluoromethylation of Imidazopyridines and Quinoxalines;The Journal of Organic Chemistry;2023-07-20
3. Recent Developments in Direct C–H Functionalization of Quinoxalin-2(1H)-Ones via Heterogeneous Catalysis Reactions;Molecules;2023-06-27
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