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 V.K. Vladimir, G.B. Alicia, Recent developments in the design and synthesis of hybrid molecules based on aminoquinoline ring and their antiplasmodial evaluation, Eur. J. Med. Chem. 44 (2009) 3091-3113.
 R.O. Kennedy, R.D. Thomas, Coumarins: Biology, Applications and Mode of Action, Wiley & Sons, Chichester, (1997).
 M. Kawase, B. Varu, A. Shah, N. Motohashi, S. Tani, S. Saito, S. Debnath, S. Mahapatra, S.G. Dastidar, A.N. Chakrabarty, Antimicrobial activity of new coumarin derivatives, Arzneimittelforschung. 51 (2001) 67-71.
 K.B. Vyas, K.S. Mimavat, G.R. Jani, M.V. Hathi, Synthesis and antimicrobial activity of coumarin derivatives metal complex; An in vitro evaluation, Orbital. 1 (2009) 183-192.
 S. Bairagi, A. Bhosale, M.N. Deodhar, Design, Synthesis and Evaluation of Schiff's Bases of 4-Chloro-3-coumarin aldehyde as Antimicrobial Agents, E-J. Chem. 6 (2009) 759-762.
 S.E. Lopez, M.E. Rosales, C.E. Canelon, E.A. Valverode, R.C. Narvaez, J.E. Charris, F.A. Giannini, R.D. Enriz, M. Carrasco, S. Zacchino, Synthesis and preliminary cytotoxic and antifungal evaluation of some 6-n, n-dialkyl 2-aryl-4(3h)-quinazolinone derivatives, Hetrocycl. Commun. 7 (2000).
 K.M. Khan, S.S. Zafar, Z.K. Muhammad, Zia-Ullah, C.M. Iqbal, Atta-ur-Rahman, P. Shahnaz, H.C. Zahid, T.S. Claudiu, Synthesis of coumarin derivatives with cytotoxic, antibacterial and antifungal activity, Enzyme Inhib. Med. Chem. 19 (2004) 373-379.
 Y. Bansal, P. Sethi, G. Bansal, Coumarin: a potential nucleus for anti-inflammatory molecules, Med. Chem. Res. 22 (2013) 3049-3060.
 K.C. Fylaktakidou, D.J. Hadjipavlou-Litina, K.E. Litinas, D.N. Nicolaides, Natural and synthetic coumarin derivatives with anti-inflammatory/antioxidant activities, Curr. Pharm. Des. 10 (2004) 3813-3833.
 M.A. Musa, J.S. Cooperwood, M.O.F. Khan, A review of coumarin derivatives in pharmacotherapy of breast cancer, Curr. Med. Chem. 15 (2008) 2664-2679.
 C. Kontogiorgis, A. Detsi, D. Hadjipavlou-Litina, Coumarin-based drugs: a patent review, Expert Opin. Ther. Patents. 22 (2012) 437-454.
 P.O. Patil, S.B. Bari, S.D. Firke, P.K. Deshmukh, S.T. Donda, D.A. Patil, A comprehensive review on synthesis and designing aspects of coumarin derivatives as monoamine oxidase inhibitors for depression and Alzheimer's disease, Bioorg. Med. Chem. 21 (2013).
 S.V. Dekic, V.S. Dekic, B.R. Dekic, M.S. Dekic, Synthesis of new condensed and cyclized coumarin derivatives, Chemical Papers. 61 (2007) 233-235.
 W.B. Choi, I.N. Houpis, H.R.O. Churchill, A. Molina, J.E. Lynch, R.P. Volante, P.J. Reider, A.O. King, A practical synthesis of the 5-chloromethyl-furo[2, 3-b]pyridine pharmacophores, Tetrahedron Lett. 36 (1995) 4571-4574.
 M. Bhupathy, D.A. Conlon, K.M. Wells, J.R. Nelson, P.J. Reider, K. Rossen, J.W. Sager, R.P. Volante, B.D. Dorsey, J.M. Hoffman, S.A. Joseph, S.L.J. McDaniel, A practical synthesis of 5-(chloromethyl)furo[2, 3-b]pyridine, a key intermediate for the HIV protease inhibitor, Heterocycl. Chem. 32 (1995).
 C.O. Kappe, T. Kappe, Synthesis of substituted 3-pyridinecarbonitriles with potential biological activity, Monatsh. Chem. 120 (1989) 1095-1100.
 G. Ozturk, D.D. Erol, T. Uzbay, M.D. Aytemir, Synthesis of 4(1H)-pyridinone derivatives and investigation of analgesic and anti-inflammatory activities, Farmaco. 56 (2001) 251-256.
 A. Abadi, O. Al-Deeb, A. Al-Afify, H. El-Kashef, Synthesis of 4-alkyl (aryl)-6-aryl-3-cyano-2(1H)-pyridinones and their 2-imino isosteres as nonsteroidal cardiotonic agents, Farmaco. 54 (1999) 195-201.
 P. Storck, A. Aubertin, D.S. Grierson, Tosylation/mesylation of 4-hydroxy-3-nitro-2-pyridinones as an activation step in the construction of dihydropyrido [3, 4b] benzo [f] [1, 4]thiazepin-1-one based anti-HIV agents, Tetrahedron Lett. 46 (2005).
 A. Evidente, M. Fiore, G. Bruno, L. Sparapano, A. Motta, Chemical and biological characterisation of sapinopyridione, a phytotoxic 3, 3, 6-trisubstituted-2, 4-pyridione produced by Sphaeropsis sapinea, a toxigenic pathogen of native and exotic conifers and its derivatives, Phytochemistry. 67 (2006).
 M.T. Cocco, C. Congiu, V. Onnis, New bis(pyridyl)methane derivatives from 4-hydroxy-2-pyridones: synthesis and antitumoral activity, Eur. J. Med. Chem. 38 (2003) 37-47.
 Q. Li, L.A. Mitscher, L.L. Shen, The 2-pyridone antibacterial agents: bacterial topoisomerase inhibitors, Med. Res. Rev. 20 (2000) 231-293.
 L.A. Mitscher, Bacterial topoisomerase inhibitors: quinolone and pyridone antibacterial agents, Chem. Rev. 105 (2005) 559-592.
 N.C. Desai, N. Bhatt, A. Dodiya, T. Karkar, B. Patel, M. Bhatt, Synthesis, characterization and antimicrobial screening of thiazole based 1, 3, 4-oxadiazoles heterocycles, Res. Chem. Intermed. (2015).
 N.C. Desai, N.R. Shihory, G.M. Kotadiya, P. Desai, Synthesis, antibacterial and antitubercular activities of benzimidazole bearing substituted 2-pyridone motifs, Eur. J. Med. Chem. 82 (2014) 480-489.
 N.C. Desai, N. Shihory, M. Bhatt, B. Patel, T. Karkar, Studies on antimicrobial evaluation of some 1-(1-(1h-benzo[d]imidazol-2-yl)ethylidene)amino)-6-(arylidene) amino)-2-oxo-4-phenyl-1, 2-dihydropyridine-3, 5-dicarbonitriles, Synth. Commun. 45 (2015).
 National committee for clinical laboratory, Standards Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically approved standard, third ed. NCCLS Publication M7-A3, Villanova, PA, (1993).
 National committee for clinical laboratory standards, Reference Method for Broth Dilution Antifungal Testing of Yeasts, Proposed Standard, NCCLS Document M27-P; Villanova, PA, (1992).
 N.C. Desai, V.V. Joshi, K.M. Rajpara, H.V. Vaghani, H.M. Satodiya, Facile synthesis of novel fluorine containing pyrazolebased thiazole derivatives and evaluation of antimicrobial activity, J. Fluorine Chem. 142 (2012) 67-78.
 N.C. Desai, K.M. Rajpara, V.V. Joshi, Synthesis and characterization of some new quinoline based derivatives endowed with broad spectrum antimicrobial potency, Bioorg. Med. Chem. Lett. 22 (2012) 6871- 6875.
 N. Desai, N. Bhatt, S. Joshi, "Synthetic modifications in ethyl 2-amino-4-methylthiazole-5-carboxylate: 3D QSAR analysis and antimicrobial study", Synthetic Communications, p. 1, 2019DOI: https://doi.org/10.1080/00397911.2019.1587777