- Jain P.K. and Joshi H. Coumarin: chemical and pharmacological profile. Appl. Pharm. Sci. 2: 236-240 (2012).
- Murray R.D.H. In Progress in the Chemistry of Organic Natural Products. Springer: Wien-New York. 72: 1-119 (1997).
- Charitos C., Kokotos G. and Tzougraki C. Bifunctional coumarin derivatives in solution and solid phase synthesis of fluorogenic enzyme substrates. Heterocycl. Chem. 38: 153-158 (2001).
- Borges F., Roleira F., Milhazes N., Santana L. and Uriarte E. Simple coumarins and analogues in medicinal chemistry: occurrence, synthesis and biological activity. Med. Chem. 12: 887-916 (2005).
- Gurumurthy Ch., Fatima N., Reddy G.N., Ganesh Kumar C., Sabitha G. and Ramakrishna, K.V.S. A diastereoselective synthesis of tetrahydro- and dihydro-pyrido[2,3-c]coumarin derivatives via a one-pot three-component Povarov reaction catalyzed by bismuth(III) chloride. Med. Chem. Lett. 26: 5119-5125 (2016).
- Chen Z., Hua L. and Peng F. Efficient Synthesis of Functionalized Pyrido[2,3-c]coumarin Derivatives by a One-Pot Three-Component Reaction. Synlett, 27: 1888-1892 (2016).
- Khan A.T. and Das D.K. Michael Initiated Ring Closure (MIRC) reaction on in situ generated benzylidenecyclohexane-1,3-diones for the construction of chromeno[3,4-b]quinoline derivatives. Tetrahedron Lett. 53: 2345-2351 (2012).
- Madhura V., Kulkarni M.V., Shah A. and Alagawadi K.R. Mannich Reaction as a New Route for the Synthesis of Tetrahydro Pyrimido Benzimidazolyl Coumarins. Heterocycl. Chem. 51: 1705-1711 (2014).
- Yu T., Peng Z., Yuling Z., Hui Z., Jing M. and Duowang F. Synthesis, characterization and high-efficiency blue electroluminescence based on coumarin derivatives of 7-diethylaminocoumarin-3-carboxamide. Electron. 10: 653-660 (2009).
- Asish R., Arunima M. and Raghunath S. Synthesis of biologically potent new 3-(heteroaryl) aminocoumarin derivatives via Buchwald–Hartwig C–N coupling. Tetrahedron Lett. 51: 1099-1102 (2010).
- Amit A., Jamie K., Chad C., Natasha D. and Graham J. Hydrolysis-free synthesis of 3-aminocoumarins. Tetrahedron Lett. 48: 5077-5080 (2007).
- Viña D., Matos M.J., Yáñez M., Santana L. and Uriarte E. 3-Substituted coumarins as dual inhibitors of AChE and MAO for the treatment of Alzheimer's disease. Chem. Comm. 3: 213-218 (2010).
- Kadhum A.A., Mohamad A.B., Al-Amiery A.A. and Takriff M.S. Antimicrobial and antioxidant activities of new metal complexes derived from 3-aminocoumarin. Molecules, 16: 6969-6984 (2011).
- Hamama W.S., Ibrahim M.E., Metwalli A.E. and Zoorob H.H. Recent synthetic aspects on the chemistry of aminocoumarins. Chem. Intermediat. 43: 5943-5983 (2017).
- Meng T., Zou Y., Khorev O., Jin Y., Zhou H., Zhang Y., Hu D., Ma L., Wang X. and Shen J. Simple and Efficient Copper (I)-Catalyzed Access to Three Versatile Aminocoumari-Based Scaffolds using Isocyanoacetate. Synth. Catal. 353: 918-924 (2011).
- Linch F.W. Chem. Soc. Trans. 101: 1759-1765 (1912).
- Messaoudi S., Brion J.D. and Alami M. An Expeditious Copper-Catalyzed Access to 3-Aminoquinolinones, 3-Aminocoumarins and Anilines using Sodium Azide. Synth. Catal. 352: 1677-1687 (2010).
- Wan X. and Joullie M.M. Enantioselective total syntheses of trichodermamides A and B. Am. Chem. Soc. 130: 17236-17237 (2008).
-
- Abdshahzadeh H., Golshani M., Nadri H., Saberi Kia I., Abdolahi Z., Forootanfar H., Ameri A., Tüylü Küçükkılınç T., Ayazgok B., Jalili-Baleh L., Sadat Ebrahimi S.E., Moghimi S., Haririan I., Khoobi M. and Foroumadi A. 3-Aryl Coumarin Derivatives Bearing Aminoalkoxy Moiety as Multi-Target-Directed Ligands against Alzheimer's Disease. Biodivers. 16: e1800436 (2019).
- Khan M.A. and Gemal A.L. Synthesis of 5H[1]benzopyrano[3,4-b]pyridine-5-one and its derivatives. Heterocycl. Chem. 14: 1009-1012 (1977)
- Firoozpour L., Yahyavi H., Ejtemaei R., Moghimi S. and Foroumadi A. A one-pot, three-component, solvent-free synthesis of novel 6h-chromeno[3’,4’:5,6]pyrido[2,3-d]pyrimidine-triones under microwave irradiation. Chem. Res. 42: 604-607 (2018).
- Nikookar H., Moghimi S., Sayahi M.H., Mahdavi M., Ranjbar P.R. Firoozpour L. and Foroumadi A. A Convenient Method for the Synthesis of Chromeno[4,3-b]pyridines Via Three-component Reaction. Chem. High Throughput Screen. 21: 344-348 (2018).
- Firoozpour L., Nikookar H., Moghimi S., Mahdavi M., Asadipour A. and Ranjbar P.R. An efficient approach to the synthesis of coumarin-fused dihydropyridinones. Commun. 23: 305-308 (2017).
- Yahya-Meymandi A., Nikookar H., Moghimi S., Mahdavi M., Firoozpour, L., Asadipour A., Ranjbar P.R. and Foroumadi A. An efficient four-component reaction for the synthesis of chromeno[4,3-b]quinolone. Iran. Chem. Soc. 14: 771-775 (2016).
- Akbarzadeh T., Rafinejad A., Fallah-Tafti A., Tiwari R., Nasrolahi Shirazi A., Mandal D., Parang K. and Foroumadi A. Synthesis and Evaluation of Ethyl 2, 4-dioxo-4-arylbutanoate Derivatives as Src Kinase Inhibitors. Sci. I. R. Iran. 26: 321-325 (2015).
- Das D.K., Sarkar S., Khan M., Belal M. and Khan A.T. A mild and efficient method for large scale synthesis of 3-aminocoumarins and its further application for the preparation of 4-bromo-3-aminocoumarins. Tetrahedron Lett. 55: 4869-4874 (2014).
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