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For: Jiang X, Wu K, Bai R, Zhang P, Zhang Y. Functionalized quinoxalinones as privileged structures with broad-ranging pharmacological activities. Eur J Med Chem 2022;229:114085. [PMID: 34998058 DOI: 10.1016/j.ejmech.2021.114085] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
Number Citing Articles
1 Zhang L, He J, Shen J, Xu H, Zhu D, Shen C. Highly efficient synthesis of C3-heteroaryl 3-fluorooxindoles via a one-pot stepwise Ce(iii)/photoassisted cross-dehydrogenative coupling/fluorooxidation process. Org Chem Front 2023. [DOI: 10.1039/d2qo01599d] [Reference Citation Analysis]
2 Li Y, Song GT, Tang DY, Xu ZG, Chen ZZ. Acid-Promoted Direct C-H Carbamoylation at the C-3 Position of Quinoxalin-2(1H)-ones with Isocyanide in Water. ACS Omega 2023;8:1577-87. [PMID: 36643431 DOI: 10.1021/acsomega.2c06946] [Reference Citation Analysis]
3 Suriya U, Mahalapbutr P, Wimonsong W, Yotphan S, Choowongkomon K, Rungrotmongkol T. Quinoxalinones as A Novel Inhibitor Scaffold for EGFR (L858R/T790M/C797S) Tyrosine Kinase: Molecular Docking, Biological Evaluations, and Computational Insights. Molecules 2022;27. [PMID: 36558033 DOI: 10.3390/molecules27248901] [Reference Citation Analysis]
4 Lu Y, Zhang Z, Wu H, Zhou M, Song H, Ji H, Jiang J, Chen J, He W. TBAI/H2O-cooperative electrocatalytic decarboxylation coupling-annulation of quinoxalin-2(1H)-ones with N-arylglycines. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.108036] [Reference Citation Analysis]
5 Stern N, Gacs A, Tátrai E, Flachner B, Hajdú I, Dobi K, Bágyi I, Dormán G, Lőrincz Z, Cseh S, Kígyós A, Tóvári J, Goldblum A. Dual Inhibitors of AChE and BACE-1 for Reducing Aβ in Alzheimer’s Disease: From In Silico to In Vivo. IJMS 2022;23:13098. [DOI: 10.3390/ijms232113098] [Reference Citation Analysis]
6 More DA, Mujahid M, Muthukrishnan M. Metal‐ And Light‐Free Direct C‐3 Ketoalkylation of Quinoxalin‐2(1 H )‐Ones with Cyclopropanols in Aqueous Medium. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202203597] [Reference Citation Analysis]
7 Kumar A, Dhameliya TM, Sharma K, Patel KA, Hirani RV, Bhatt AJ. Sustainable approaches towards the synthesis of quinoxalines: An update. Journal of Molecular Structure 2022;1259:132732. [DOI: 10.1016/j.molstruc.2022.132732] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Zhang L, He J, Zhang P, Zhu D, Zheng K, Shen C. Visible-light-induced C–H sulfenylation of quinoxalin-2(1H)-ones with disulfides by sustainable cerium catalysis. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.04.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Jiang J, Song S, Guo J, Zhou J, Li J. Mechanically induced transition metal free C(sp)-H arylation of quinoxalin(on)es with diaryliodonium salts and piezoelectric BaTiO3. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153820] [Reference Citation Analysis]
10 Thabet FM, Dawood KM, Ragab EA, Nafie MS, Abbas AA. Design and synthesis of new bis(1,2,4-triazolo[3,4- b ][1,3,4]thiadiazines) and bis((quinoxalin-2-yl)phenoxy)alkanes as anti-breast cancer agents through dual PARP-1 and EGFR targets inhibition. RSC Adv 2022;12:23644-60. [DOI: 10.1039/d2ra03549a] [Reference Citation Analysis]
11 Xuan L, Du R, Lei P, Zhao W, Tan L, Ni C, Wang H, Yan Q, Wang W, Chen F. Remote C(sp3)–H heteroarylation of N-fluorocarboxamides with quinoxalin-2(1H)-ones under visible-light-induced photocatalyst-free conditions. Green Chem 2022. [DOI: 10.1039/d2gc02874c] [Reference Citation Analysis]