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For: Mermer A, Keles T, Sirin Y. Recent studies of nitrogen containing heterocyclic compounds as novel antiviral agents: A review. Bioorg Chem 2021;114:105076. [PMID: 34157555 DOI: 10.1016/j.bioorg.2021.105076] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Hussein BRM, Moustafa AH. Utility of arylglyoxal hydrates in synthesis of 4-aroyl-[1,3,5]triazino[1,2-a]benzimidazol-2(1H)-imines and 5-aryl-2-phenyl-4H-imidazol-4-imines. Mol Divers 2022. [PMID: 35064443 DOI: 10.1007/s11030-022-10379-8] [Reference Citation Analysis]
2 Parsa Habashi B, Poursattar Marjani A. N-methylpyrrolidine as an effective organocatalyst for the regioselective synthesis of 3-hydroxy-3,5/6-di-aryl-1H-imidazo[1,2-a]imidazol-2(3H)-ones. Res Chem Intermed 2022;48:2325-36. [DOI: 10.1007/s11164-022-04717-6] [Reference Citation Analysis]
3 Mishra S, Nair SR, Baire B. Recent approaches for the synthesis of pyridines and (iso)quinolines using propargylic Alcohols. Org Biomol Chem 2022. [PMID: 35678139 DOI: 10.1039/d2ob00587e] [Reference Citation Analysis]
4 Sun Z, Huang H, Wang Q, Huang C, Mao G, Deng G. Visible light-mediated radical-cascade addition/cyclization of arylacrylamides with aldehydes to form quaternary oxindoles at room temperature. Org Chem Front 2022;9:3506-14. [DOI: 10.1039/d2qo00319h] [Reference Citation Analysis]
5 Jeelan Basha N, Basavarajaiah SM, Shyamsunder K. Therapeutic potential of pyrrole and pyrrolidine analogs: an update. Mol Divers. [DOI: 10.1007/s11030-022-10387-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Baidya M, Mallick S, De Sarkar S. Regioselective Synthesis of N2-Aryl 1,2,3-Triazoles via Electro-oxidative Coupling of Enamines and Aryldiazonium Salts. Org Lett 2022. [PMID: 35112868 DOI: 10.1021/acs.orglett.1c04099] [Reference Citation Analysis]
7 Tao LF, Zhang S, Huang F, Wang WT, Luo ZH, Qian L, Liao JY. Diastereo- and Enantioselective Silver-Catalyzed [3+3] Cycloaddition and Kinetic Resolution of Azomethine Imines with Activated Isocyanides. Angew Chem Int Ed Engl 2022;61:e202202679. [PMID: 35289973 DOI: 10.1002/anie.202202679] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Singh PR, Gopal B, Kumar M, Goswami A. A metal-free BF3·OEt2 mediated chemoselective protocol for the synthesis of propargylic cyclic imines. Org Biomol Chem 2022;20:4933-41. [PMID: 35648486 DOI: 10.1039/d2ob00530a] [Reference Citation Analysis]
9 Tao L, Zhang S, Huang F, Wang W, Luo Z, Qian L, Liao J. Diastereo‐ and Enantioselective Silver‐Catalyzed [3+3] Cycloaddition and Kinetic Resolution of Azomethine Imines with Activated Isocyanides. Angewandte Chemie. [DOI: 10.1002/ange.202202679] [Reference Citation Analysis]
10 Ren M, Sun S, Wu Y, Shi Y, Wang ZJ, Cao H, Xie Y. The structure-activity relationship of aromatic compounds in advanced oxidation processes:a review. Chemosphere 2022;:134071. [PMID: 35216974 DOI: 10.1016/j.chemosphere.2022.134071] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Niu Z, Ma S, Zhang L, Liu Q, Zhang S. Discovery of Novel Quinazoline Derivatives as Potent Antitumor Agents. Molecules 2022;27:3906. [PMID: 35745027 DOI: 10.3390/molecules27123906] [Reference Citation Analysis]
12 Suć Sajko J, Jerić I. Synthesis of Nβ-Substituted 1,2-Diazetidin-3-ones by the Ugi Reaction Comprising Chiral α-Hydrazino Acids. J Org Chem 2022. [PMID: 35549347 DOI: 10.1021/acs.joc.2c00238] [Reference Citation Analysis]
13 Huang W, Wang Y, Xu S, Qiao H, Cheng H, Wang L, Liu S, Tian Q, Wang R, Wang H, Bi Y. Design, synthesis, and tumor drug resistance reversal activity of novel hederagenin derivatives modified by nitrogen-containing heterocycles. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114207] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Zhong L, Wang J, Zhu S, Chen S, Peng D. Crystal structure of 3-(difluoromethyl)-1-methyl- N -(4,11,11-trimethyl-1,2,3,4-tetrahydro-1,4-methanoacridin-9-yl)-1 H -pyrazole-4-carboxamide monohydrate, C 23 H 26 F 2 N 4 O 3. Zeitschrift für Kristallographie - New Crystal Structures 2022;0. [DOI: 10.1515/ncrs-2022-0030] [Reference Citation Analysis]
15 Yu Y, Ding J, Zhou Y, Xiao H, Wu G. Biosafety chemistry and biosafety materials: a new perspective to solve biosafety problems. Biosaf Health 2022. [PMID: 35013725 DOI: 10.1016/j.bsheal.2022.01.001] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
16 Sharma S, Utreja D. Synthesis and antiviral activity of diverse heterocyclic scaffolds. Chem Biol Drug Des 2021. [PMID: 34551197 DOI: 10.1111/cbdd.13953] [Reference Citation Analysis]
17 De S, Aamna B, Sahu R, Parida S, Behera SK, Dan AK. Seeking heterocyclic scaffolds as antivirals against dengue virus. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114576] [Reference Citation Analysis]
18 Shu Y, Chen M, Lu D, Zhou Z, Yu J, Hu X, Yang J, Li A, Liu J, Luo H. Synthesis and Bioactivities of Novel Galactoside Derivatives Containing 1,3,4-Thiadiazole Moiety. Front Chem 2022;10:910710. [DOI: 10.3389/fchem.2022.910710] [Reference Citation Analysis]
19 Akhlaghi S, Mostoufi A, Kalantar H, Fereidoonnezhad M. Synthesis and biological evaluations of novel pyrazinoic acid derivatives as anticancer agents. Med Chem Res. [DOI: 10.1007/s00044-022-02858-2] [Reference Citation Analysis]
20 Dai R, Li T, Xiao S, Chen Y, Gao J, Su G, Zhao Y. Synthesis of panaxadiol thiadiazole derivatives and study on its potential cell cycle arrest. Journal of Molecular Structure 2022;1264:133208. [DOI: 10.1016/j.molstruc.2022.133208] [Reference Citation Analysis]
21 Farghaly TA, Alsaedi AMR, Alenazi NA, Harras MF. Anti-viral activity of thiazole derivatives: an updated patent review. Expert Opinion on Therapeutic Patents. [DOI: 10.1080/13543776.2022.2067477] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Wang Y, Qin K, Wang R, Zhang W, Zhong Q. Crystal structure of ( E )-1-(4-benzyl-3,5-dioxomorpholin-2-ylidene)ethyl acetate, C 15 H 15 N 1 O 5. Zeitschrift für Kristallographie - New Crystal Structures 2022;0. [DOI: 10.1515/ncrs-2021-0450] [Reference Citation Analysis]
23 Samanta A, Pramanik S, Mondal S, Maity S. Zinc acetate-promoted blocking of the ATRA process with alkyl halides enabling photochemical alkylamination of olefins. Chem Commun (Camb) 2022;58:8400-3. [PMID: 35796040 DOI: 10.1039/d2cc02574d] [Reference Citation Analysis]
24 Li M, Gao Y, Xu K, Zhang Y, Gong S, Wang Z, Wang S. Rational design and comparison of three benzazole-based fluorescent probes for sensitively and reversibly detecting BF3. Dyes and Pigments 2022;205:110558. [DOI: 10.1016/j.dyepig.2022.110558] [Reference Citation Analysis]
25 Mustafa G, Zia-ur-rehman M, Sumrra SH, Ashfaq M, Zafar W, Ashfaq M. A critical review on recent trends on pharmacological applications of pyrazolone endowed derivatives. Journal of Molecular Structure 2022;1262:133044. [DOI: 10.1016/j.molstruc.2022.133044] [Reference Citation Analysis]
26 Lan W, Tang X, Yu J, Fei Q, Wu W, Li P, Luo H. Design, Synthesis, and Bioactivities of Novel Trifluoromethyl Pyrimidine Derivatives Bearing an Amide Moiety. Front Chem 2022;10:952679. [DOI: 10.3389/fchem.2022.952679] [Reference Citation Analysis]
27 Mohi El-deen EM, Anwar MM, El-gwaad AAA, Karam EA, El-ashrey MK, Kassab RR. Novel Pyridothienopyrimidine Derivatives: Design, Synthesis and Biological Evaluation as Antimicrobial and Anticancer Agents. Molecules 2022;27:803. [DOI: 10.3390/molecules27030803] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
28 Qiu J, Yuan D, Yu J, Zhang Y, Li W, Tang Z, He P, Ren Z. A Facile Synthesis of Indole Derivatives by a Palladium‐Catalyzed Process Initiated from Ugi Adducts and their Antifungal Activities. ChemistrySelect 2021;6:12921-5. [DOI: 10.1002/slct.202104070] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Obaid RJ, Naeem N, Mughal EU, Al-rooqi MM, Sadiq A, Jassas RS, Moussa Z, Ahmed SA. Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesterase. RSC Adv 2022;12:19764-855. [DOI: 10.1039/d2ra03081k] [Reference Citation Analysis]