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For: Auti PS, George G, Paul AT. Recent advances in the pharmacological diversification of quinazoline/quinazolinone hybrids. RSC Adv 2020;10:41353-92. [DOI: 10.1039/d0ra06642g] [Cited by in Crossref: 56] [Cited by in F6Publishing: 60] [Article Influence: 18.7] [Reference Citation Analysis]
Number Citing Articles
1 Ramarao S, Pothireddy M, Venkateshwarlu R, Moturu KMV, Siddaiah V, Kapavarapu R, Dandela R, Pal M. A rapid construction of 4(3H)-quinazolinone and related ring under ultrasound irradiation: In silico/in vitro studies of compounds synthesized. Journal of Molecular Structure 2023;1273:134280. [DOI: 10.1016/j.molstruc.2022.134280] [Reference Citation Analysis]
2 Lin Hu Y, Rong Q, Chen C, Bing Liu X. Sustainable and efficient 2,3-dihydroquinazolin-4(1H)-ones production over heterogeneous and recyclable Al-MCM-41 supported dual imidazolium ionic liquids nanocomposites. Journal of Saudi Chemical Society 2023;27:101588. [DOI: 10.1016/j.jscs.2022.101588] [Reference Citation Analysis]
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4 Skoptsova AA, Shestakov AS, Ledenyova IV, Stolpovskaya NV, Podoplelova NA, Panteleev MA, Paponov BV, Sidorenko OE, Shikhaliev KS, Novichikhina NP. Reaction of 1‐Phenacylidene pyrrolo[3,2,1‐ ij ]quinolin‐2‐ones with Cyclic/Acyclic Enaminones and the Anticoagulant Activity of Synthesized Pyrrole‐Quinoline Derivatives. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200730] [Reference Citation Analysis]
5 Zayed MF. Medicinal Chemistry of Quinazolines as Analgesic and Anti-Inflammatory Agents. ChemEngineering 2022;6:94. [DOI: 10.3390/chemengineering6060094] [Reference Citation Analysis]
6 Ziarani GM, Ashtiani ST, Mohajer F, Badiei A, Gaikwad SV, Varma RS. 2,3-Dihydro-Quinazolin-4(1H)-One as a Fluorescent Sensor for Hg2+ Ion and its Docking Studies in Cancer Treatment. Chemistry-Didactics-Ecology-Metrology 2022;27:25-33. [DOI: 10.2478/cdem-2022-0004] [Reference Citation Analysis]
7 Madhava Reddy M, Desikan R, Naik S, Kumar S, Kumar D T, Priya Doss C G, Sivaramakrishna A. Designing, Synthesis, and Anti-Breast Cancer Activity of a Series of New Quinazolin-4(1H)-one Derivatives. Chem Biodivers 2022;19:e202200662. [PMID: 36261320 DOI: 10.1002/cbdv.202200662] [Reference Citation Analysis]
8 Sain S, Jaiswal S, Jain S, Misra N, Srivastava A, Jendra R, Kishore D, Dwivedi J, Wabaidur SM, Islam MA, Sharma S. Synthesis and Theoretical Studies of Biologically Active Thieno Nucleus Incorporated Tri and Tetracyclic Nitrogen Containing Heterocyclics Scaffolds via Suzuki Cross-Coupling Reaction. Chem Biodivers 2022;19:e202200540. [PMID: 36310125 DOI: 10.1002/cbdv.202200540] [Reference Citation Analysis]
9 Jin L, Le Z, Fan Q, Yang J, Zhang C, Li Q, Xie Z. Fast quinazolinone synthesis by combining enzymatic catalysis and photocatalysis. Photochem Photobiol Sci 2022. [DOI: 10.1007/s43630-022-00332-x] [Reference Citation Analysis]
10 Emami L, Khabnadideh S, Faghih Z, Farahvasi F, Zonobi F, Gheshlaghi SZ, Daili S, Ebrahimi A, Faghih Z. Synthesis, biological evaluation, and computational studies of some novel quinazoline derivatives as anticancer agents. BMC Chem 2022;16:100. [PMID: 36419100 DOI: 10.1186/s13065-022-00893-z] [Reference Citation Analysis]
11 Moheb M, Iraji A, Dastyafteh N, Khalili Ghomi M, Noori M, Mojtabavi S, Faramarzi MA, Rasekh F, Larijani B, Zomorodian K, Sadat-ebrahimi SE, Mahdavi M. Synthesis and bioactivities evaluation of quinazolin-4(3H)-one derivatives as α-glucosidase inhibitors. BMC Chemistry 2022;16:97. [DOI: 10.1186/s13065-022-00885-z] [Reference Citation Analysis]
12 Wang F, Peng B, Ren T, Liu S, Du J, Chen Z, Zhang T, Gu X, Li M, Cao S, Xu X. A 1,2,3-Triazole Derivative of Quinazoline Exhibits Antitumor Activity by Tethering RNF168 to SQSTM1/P62. J Med Chem 2022. [DOI: 10.1021/acs.jmedchem.2c00432] [Reference Citation Analysis]
13 Chen XW, Rao L, Chen JL, Zou Y. Unexpected assembly machinery for 4(3H)-quinazolinone scaffold synthesis. Nat Commun 2022;13:6522. [PMID: 36316336 DOI: 10.1038/s41467-022-34340-3] [Reference Citation Analysis]
14 Mikra C, Melissari Z, Kokotou MG, Gritzapis P, Fylaktakidou KC. Microwave-assisted synthesis of hydroxamic acid incorporated quinazolin-4[3H]-one derivatives. Sustainable Chemistry and Pharmacy 2022;29:100772. [DOI: 10.1016/j.scp.2022.100772] [Reference Citation Analysis]
15 Borah B, Swain S, Patat M, Chowhan LR. Recent advances and prospects in the organocatalytic synthesis of quinazolinones. Front Chem 2022;10:991026. [DOI: 10.3389/fchem.2022.991026] [Reference Citation Analysis]
16 Xu R, Wang Z, Zheng Q, Patil P, Dömling A. A Bifurcated Multicomponent Synthesis Approach to Polycyclic Quinazolinones. J Org Chem 2022. [PMID: 36095044 DOI: 10.1021/acs.joc.2c01561] [Reference Citation Analysis]
17 Rhazi Y, Chalkha M, Nakkabi A, Hammoudan I, Akhazzane M, Bakhouch M, Chtita S, El Yazidi M. Novel Quinazolinone–Isoxazoline Hybrids: Synthesis, Spectroscopic Characterization, and DFT Mechanistic Study. Chemistry 2022;4:969-982. [DOI: 10.3390/chemistry4030066] [Reference Citation Analysis]
18 Ibrahim ZY, Uzairu A, Shallangwa GA, Abechi SE, Isyaku S. Virtual screening and molecular dynamic simulations of the antimalarial derivatives of 2-anilino 4-amino substituted quinazolines docked against a Pf-DHODH protein target. Egypt J Med Hum Genet 2022;23. [DOI: 10.1186/s43042-022-00329-2] [Reference Citation Analysis]
19 Liu S, Wang AJ, Li M, Zhang J, Yin GD, Shu WM, Yu WC. Rh(III)-Catalyzed Tandem Reaction Access to (Quinazolin-2-yl)methanone Derivatives from 2,1-Benzisoxazoles and α-Azido Ketones. J Org Chem 2022. [PMID: 35938613 DOI: 10.1021/acs.joc.2c01214] [Reference Citation Analysis]
20 Wu Q, Deng Z, Xie D, Liu Y, Yang Q, Fu Y, Peng Y. Aminothiolation of 2-(2-bromophenyl)quinazolinones with elemental sulfur to access 7H-benzo[4,5]isothiazolo[3,2-b]quinazolinones through C–S/S–N bond formation under metal-free condition. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132911] [Reference Citation Analysis]
21 Moshkina TN, Nosova EV, Kopotilova AE, Savchuk MI, Nikonov IL, Kopchuk DS, Slepukhin PA, Kim GA, Lipunova GN, Charushin VN. Synthesis and photophysical properties of pyridyl- and quinolinyl-substituted 4-(4-aminophenyl)quinazolines. Journal of Photochemistry and Photobiology A: Chemistry 2022;429:113917. [DOI: 10.1016/j.jphotochem.2022.113917] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Galehban MH, Zeynizadeh B, Mousavi H. Introducing Fe3O4@SiO2@KCC-1@MPTMS@CuII catalytic applications for the green one-pot syntheses of 2-aryl(or heteroaryl)-2,3-dihydroquinazolin-4(1H)-ones and 9-aryl-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-diones. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134017] [Reference Citation Analysis]
23 Mori NP, Parmar PK, Khedkar VM, Khunt RC. Synthesis of N-Methylene Linker Containing Phthalimide Bearing-1 H -1,2,3-Triazole by Click Chemistry Approach: Anticancer Activity in Human Cells. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2101487] [Reference Citation Analysis]
24 Hwu JR, Roy A, Tsay S, Huang W, Lin C, Hwang KC, Hu Y, Shieh F, Leyssen P, Neyts J. Computer-Aided Design and Synthesis of (Functionalized quinazoline)–(α-substituted coumarin)–arylsulfonate Conjugates against Chikungunya Virus. IJMS 2022;23:7646. [DOI: 10.3390/ijms23147646] [Reference Citation Analysis]
25 Krivokolysko DS, Dotsenko VV, Bibik EY, Samokish AA, Venidiktova YS, Frolov KA, Krivokolysko SG, Pankov AA, Aksenov NA, Aksenova IV. New Hybrid Molecules Based on Sulfur-Containing Nicotinonitriles: Synthesis, Analgesic Activity in Acetic Acid-Induced Writhing Test, and Molecular Docking Studies. Russ J Bioorg Chem 2022;48:628-35. [DOI: 10.1134/s1068162022030104] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
26 George K, Elavarasan P, Ponnusamy S, Sathananthan K. Facile One-Pot Synthesis of Functionalized Quinoline-Fused Fluorescent Dihydro/Spiro-quinazolinone Derivatives. ACS Omega. [DOI: 10.1021/acsomega.2c00674] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Muthu Boopathi G, T. S. S. Synthesis, Characterisation and Antimicrobial Activity of Novel 2-Methyl-3-(2-(substituted ylidene)hydrazinyl)quinazolin-4(3H)-ones. RJPT 2022. [DOI: 10.52711/0974-360x.2022.00362] [Reference Citation Analysis]
28 Sundarraman B, Rengan R, Semeril D. NNO Pincer Ligand-Supported Palladium(II) Complexes: Direct Synthesis of Quinazolines via Acceptorless Double Dehydrogenative Coupling of Alcohols. Organometallics. [DOI: 10.1021/acs.organomet.2c00062] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
29 Borah B, Chowhan LR. Ultrasound-assisted transition-metal-free catalysis: a sustainable route towards the synthesis of bioactive heterocycles. RSC Adv 2022;12:14022-51. [PMID: 35558846 DOI: 10.1039/d2ra02063g] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
30 Salarinejad N, Dabiri M, Movahed SK. Directed aromatic C–H functionalization of N-arylcarbamates and quinazolinones catalyzed by palladium nanoparticles supported on nitrogen-doped graphene. Colloid and Interface Science Communications 2022;47:100606. [DOI: 10.1016/j.colcom.2022.100606] [Reference Citation Analysis]
31 Dehbi O, Riadi Y, Geesi MH, Anouar EH, Ibnouf EO, Azzallou R. Synthesis, Characterization, Antibacterial Evaluation, and Molecular Docking of New Quinazolinone-Based Derivatives. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2041053] [Reference Citation Analysis]
32 Mikra C, Bairaktari M, Petridi M, Detsi A, Fylaktakidou KC. Green Process for the Synthesis of 3-Amino-2-methyl-quinazolin-4(3H)-one Synthones and Amides Thereof:DNA Photo-Disruptive and Molecular Docking Studies. Processes 2022;10:384. [DOI: 10.3390/pr10020384] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Laha JK, Hunjan MK. Diversity in Heterocycle Synthesis Using α-Iminocarboxylic Acids: Decarboxylation Dichotomy. J Org Chem . [DOI: 10.1021/acs.joc.1c02110] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
34 Krivokolysko DS, Dotsenko VV, Bibik EY, Myazina AV, Krivokolysko SG, Vasilin VK, Pankov AA, Aksenov NA., Aksenova IV. Synthesis, Structure, and Analgesic Activity of 4-(5-Cyano-{4-(fur-2-yl)-1,4-dihydropyridin-3-yl}carboxamido)benzoic Acids Ethyl Esters. Russ J Gen Chem 2021;91:2588-605. [DOI: 10.1134/s1070363221120306] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
35 Jivani AJ, Lunagariya KS, Kapadiya KM, Dholaria PV, Khedkar VM, Khunt RC. A Step-By-Step Synthesis of S-Methylene Linker Containing Triazole-Benzoxazole Hybrids by Click Chemistry Approach: Anticancer Activity in Human Cells. Analytical Chemistry Letters 2022;12:44-57. [DOI: 10.1080/22297928.2021.1894604] [Reference Citation Analysis]
36 Coşkun N, Samandram R, Çetin Korukçu M. Mn(OAc)3 Induced C-4 Arylations of Quinazoline 3-Oxides with Arylboronic Acids. Synthesis 2022;54:210-216. [DOI: 10.1055/a-1577-6344] [Reference Citation Analysis]
37 Verma S, Kujur S, Sharma R, Pathak DD. Cucurbit[6]uril supported β-Ni(OH)2 nanoparticles as a heterogeneous catalyst for the synthesis of quinazolines via acceptorless dehydrogenative coupling of alcohols with nitriles. New J Chem 2022;46:21356-21365. [DOI: 10.1039/d2nj03484k] [Reference Citation Analysis]
38 Soda AK, C. S PK, Chilaka SK, E VK, Misra S, Madabhushi S. I 2 /TBHP mediated domino synthesis of 2-(2,4-dioxo-1,4-dihydroquinazolin-3(2 H )-yl)- N -aryl/alkyl benzamides and evaluation of their anticancer and docking studies. RSC Adv 2022;12:16589-98. [DOI: 10.1039/d2ra02216h] [Reference Citation Analysis]
39 Ahmad Mir S, Meher RK, Baitharu I, Nayak B. Molecular dynamic simulation, free binding energy calculation of Thiazolo-[2,3-b]quinazolinone derivatives against EGFR-TKD and their anticancer activity. Results in Chemistry 2022;4:100418. [DOI: 10.1016/j.rechem.2022.100418] [Reference Citation Analysis]
40 Jafari E, Rezaeinasab R, Khodarahmi G. Quinazolinone-based hybrids with diverse biological activities: A mini-review. J Res Med Sci 2022;27:68. [DOI: 10.4103/jrms.jrms_1025_21] [Reference Citation Analysis]
41 Sarfraz M, Wang C, Sultana N, Ellahi H, Rehman MFU, Jameel M, Akhter S, Kanwal F, Tariq MI, Xue S. 2,3-Dihydroquinazolin-4(1H)-one as a New Class of Anti-Leishmanial Agents: A Combined Experimental and Computational Study. Crystals 2022;12:44. [DOI: 10.3390/cryst12010044] [Reference Citation Analysis]
42 Mondal MA, Mondal S, Khan AA. Synthesis of Functionalized Quinazolinones via Acid‐Catalyzed Redox Neutral Reaction. ChemistrySelect 2021;6:11788-11791. [DOI: 10.1002/slct.202102976] [Reference Citation Analysis]
43 Karan R, Agarwal P, Sinha M, Mahato N. Recent Advances on Quinazoline Derivatives: A Potential Bioactive Scaffold in Medicinal Chemistry. ChemEngineering 2021;5:73. [DOI: 10.3390/chemengineering5040073] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
44 Sacramento M, Piúma LPA, Nascimento JER, Cargnelutti R, Jacob RG, Lenardão EJ, Alves D. Selective Synthesis of 2-(1,2,3-Triazoyl) Quinazolinones through Copper-Catalyzed Multicomponent Reaction. Catalysts 2021;11:1170. [DOI: 10.3390/catal11101170] [Reference Citation Analysis]
45 Jeminejs A, Novosjolova I, Bizdēna Ē, Turks M. Nucleophile-nucleofuge duality of azide and arylthiolate groups in the synthesis of quinazoline and tetrazoloquinazoline derivatives. Org Biomol Chem 2021;19:7706-23. [PMID: 34524320 DOI: 10.1039/d1ob01315g] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
46 Krivokolysko DS, Dotsenko VV, Bibik EY, Samokish AA, Venidiktova YS, Frolov KA, Krivokolysko SG, Vasilin VK, Pankov AA, Aksenov NA, Aksenova IV. New 4-(2-Furyl)-1,4-dihydronicotinonitriles and 1,4,5,6-Tetrahydronicotinonitriles: Synthesis, Structure, and Analgesic Activity. Russ J Gen Chem 2021;91:1646-1660. [DOI: 10.1134/s1070363221090073] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
47 Motoyama M, Doan TH, Hibner-Kulicka P, Otake R, Lukarska M, Lohier JF, Ozawa K, Nanbu S, Alayrac C, Suzuki Y, Witulski B. Synthesis and Structure-Photophysics Evaluation of 2-N-Amino-quinazolines: Small Molecule Fluorophores for Solution and Solid State. Chem Asian J 2021;16:2087-99. [PMID: 34107175 DOI: 10.1002/asia.202100534] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
48 Philips A, Raja D, Arumugam A, Lin W, Chandru Senadi G. Copper‐Catalyzed Oxidative C−C Cleavage of Carbohydrates: An Efficient Access to Quinazolinone Scaffolds. Asian J of Organic Chemis 2021;10:1795-800. [DOI: 10.1002/ajoc.202100317] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
49 Wang J, Ansari MF, Zhou CH. Identification of Unique Quinazolone Thiazoles as Novel Structural Scaffolds for Potential Gram-Negative Bacterial Conquerors. J Med Chem 2021;64:7630-45. [PMID: 34009979 DOI: 10.1021/acs.jmedchem.1c00334] [Cited by in Crossref: 26] [Cited by in F6Publishing: 29] [Article Influence: 13.0] [Reference Citation Analysis]
50 Balaji S, Balamurugan G, Ramesh R, Semeril D. Palladium(II) N^O Chelating Complexes Catalyzed One-Pot Approach for Synthesis of Quinazolin-4(3 H )-ones via Acceptorless Dehydrogenative Coupling of Benzyl Alcohols and 2-Aminobenzamide. Organometallics 2021;40:725-34. [DOI: 10.1021/acs.organomet.0c00814] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
51 Hussein MA, Salah El-din MM, Saleh EM, Mostafa AT, Abd-elazziz MT, Abdelrahman OM, Mahmoud AS, Moro AM, Abdel-wahab EA, Ali AA. Sildenafil (VIAGRATM): A Promising Anticancer Drug Against Certain Human Cancer Cell Lines. Asian J Chem 2021;33:1420-1424. [DOI: 10.14233/ajchem.2021.23199] [Reference Citation Analysis]
52 Huang J, Chen W, Liang J, Yang Q, Deng Z, Song Z, Peng Y. Rhodium( iii )-catalyzed annulation of 3-arylquinazolinones with alkynes via double C–H activation: an efficient route for quinolino[2,1- b ]quinazolinones. Org Chem Front 2021;8:6837-44. [DOI: 10.1039/d1qo01186c] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
53 Liu G, Yan C, Zhang Y, Zhao G, Jin X, Yang W, Niu P, Wang H. Synthesis and Biological Activities of Selenium/Thioether Quinazoline Compounds. HETEROCYCLES 2021;102. [DOI: 10.3987/com-21-14456] [Reference Citation Analysis]