[1] R. Kaur, S. Mandal, CdO Nanostructures as Acid-Base Bifunctional Heterogeneous Catalysts for Making Coumarin-3-carboxylic Acids at Room Temperature, ACS Applied Nano Materials, 7 (2024), DOI: 10.1021/acsanm.3c05932.
[2] S. Emami, S. Dadashpour, ChemInform Abstract: Current Developments of Coumarin-Based Anticancer Agents in Medicinal Chemistry, European journal of medicinal chemistry, 102 (2015) 611-630, DOI: 10.1016/j.ejmech.2015.08.033.
[3] U. Salar, K. Khan, M.I. Fakhri, S. Hussain, S. Tauseef, S. Ameer, A. Wadood, H. Khan, S. Perveen, 1,1′-Carbonyldiimidazole (CDI) Mediated Facile Synthesis, Structural Characterization, Antimicrobial Activity, and in-silico Studies of Coumarin-3-carboxamide Derivatives, Medicinal Chemistry, 13 (2017), DOI: 10.2174/1573406413666170623083116.
[4] S. Chakraborty, B. Paul, R. Natarajan, S. Majumdar, Ecofriendly Approach for the Large-Scale Synthesis of 4-Unsubstituted Coumarin-3-carboxylic Acids from o-Hydroxy-araldehydes and Meldrum’s Acid in the Water-SDS Micellar System, ChemistrySelect, 8 (2023), DOI: 10.1002/slct.202204128.
[5] G. He, X. Hua, N. Yang, L. Ji, J. Xu, L. Yang, Q. Wang, L. Ji, Synthesis and application of a “turn on” fluorescent probe for glutathione based on a copper complex of coumarin-3-carboxylic acid, RSC Advances, 6 (2016) 100727-100732.
[6] M.W. Irvine, B.M. Costa, A. Volianskis, G. Fang, L. Ceolin, G.L. Collingridge, D.T. Monaghan, D.E. Jane, Coumarin-3-carboxylic acid derivatives as potentiators and inhibitors of recombinant and native N-methyl-d-aspartate receptors, Neurochemistry International, 61 (2012) 593-600, DOI: 10.1016/j.neuint.2011.12.020.
[7] D. Markad, S. Khullar, S.K. Mandal, A Primary Amide-Functionalized Heterogeneous Catalyst for the Synthesis of Coumarin-3-carboxylic Acids via a Tandem Reaction, Inorganic Chemistry, 59 (2020) 11407-11416, DOI: 10.1021/acs.inorgchem.0c01178.
[8] M. Lončarić, D. Gašo-Sokač, S. Jokić, M. Molnar, Recent Advances in the Synthesis of Coumarin Derivatives from Different Starting Materials, Biomolecules, 10 (2020), DOI: 10.3390/biom10010151.
[9] M.M. Zeydi, S.J. Kalantarian, Z. Kazeminejad, Overview on developed synthesis procedures of coumarin heterocycles, Journal of the Iranian Chemical Society, 17 (2020) 3031-3094, DOI: 10.1007/s13738-020-01984-1.
[10] R.H. Vekariya, H.D. Patel, Recent Advances in the Synthesis of Coumarin Derivatives via Knoevenagel Condensation: A Review, Synthetic Communications, 44 (2014) 2756-2788, DOI: 10.1080/00397911.2014.926374.
[11] X. He, Y. Shang, Y. Zhou, Z. Yu, G. Han, W. Jin, J. Chen, Synthesis of coumarin-3-carboxylic esters via FeCl3-catalyzed multicomponent reaction of salicylaldehydes, Meldrum’s acid and alcohols, Tetrahedron, 71 (2015) 863-868, DOI: 10.1016/j.tet.2014.12.042.
[12] X.-S. Wang, J. Zhou, K. Yang, M.-M. Zhang, Divergent Products Obtained from the Reactions of Salicylaldehyde and 4-Hydroxycoumarin in TEBAC-H2O, KF-Al2O3-EtOH, and Ionic Liquid, Synthetic Communications, 40 (2010) 3332-3345, DOI: 10.1080/00397910903419837.
[13] B. Karami, M. Farahi, S. Khodabakhshi, Rapid Synthesis of Novel and Known Coumarin-3-carboxylic Acids Using Stannous Chloride Dihydrate under Solvent-Free Conditions, Helvetica Chimica Acta, 95 (2012) 455-460, DOI: 10.1002/hlca.201100342.
[14] G. Brahmachari, Room Temperature One-Pot Green Synthesis of Coumarin-3-carboxylic Acids in Water: A Practical Method for the Large-Scale Synthesis, ACS Sustainable Chemistry & Engineering, 3 (2015) 2350-2358, DOI: 10.1021/acssuschemeng.5b00826.
[15] F. Bigi, L. Chesini, R. Maggi, G. Sartori, Montmorillonite KSF as an Inorganic, Water Stable, and Reusable Catalyst for the Knoevenagel Synthesis of Coumarin-3-carboxylic Acids, The Journal of Organic Chemistry, 64 (1999) 1033-1035, DOI: 10.1021/jo981794r.
[16] S. Fiorito, S. Genovese, V.A. Taddeo, F. Epifano, Microwave-assisted synthesis of coumarin-3-carboxylic acids under ytterbium triflate catalysis, Tetrahedron Letters, 56 (2015) 2434-2436, DOI: 10.1016/j.tetlet.2015.03.079.
[17] S.F. da Silva, F.A.e. Silva, A.P.M. de Souza, T.S. Rodrigues, R.R. Teixeira, Preparation of NaNbO3 nanoplates and their application in the synthesis of arylidene indan-1,3-diones, functionalized C-3 isobenzofuranones and Meldrum’s acid derivatives, Journal of Materials Science, 57 (2022) 1669-1688, DOI: 10.1007/s10853-021-06725-0.
[18] A. Maleki, Z. Alirezapour, M.H. Abdollahi-Basir, M. Babaei, Fe3O4@SiO2–NH2 core-shell nanocomposite as an efficient and green catalyst for the multi-component synthesis of highly substituted chromeno[2,3-b]pyridines in aqueous ethanol media, Green Chemistry Letters and Reviews, 8 (2015) 40-49, DOI: 10.1080/17518253.2015.1107139.
[19] A. Maleki, R. Ghalavand, R. Firouzi Haji, Synthesis and characterization of the novel diamine-functionalized Fe3O4@SiO2 nanocatalyst and its application for one-pot three-component synthesis of chromenes, Applied Organometallic Chemistry, 32 (2018) e3916, DOI: 10.1002/aoc.3916.
[20] D. Elhamifar, Z. Ramazani, M. Norouzi, R. Mirbagheri, Magnetic iron oxide/phenylsulfonic acid: A novel, efficient and recoverable nanocatalyst for green synthesis of tetrahydrobenzo[b]pyrans under ultrasonic conditions, Journal of colloid and interface science, 511 (2018) 392-401, DOI: 10.1016/j.jcis.2017.10.013.
[21] R. Firouzi-Haji, A. Maleki, L-Proline-Functionalized Fe3O4 Nanoparticles as an Efficient Nanomagnetic Organocatalyst for Highly Stereoselective One-Pot Two-Step Tandem Synthesis of Substituted Cyclopropanes, ChemistrySelect, 4 (2019) 853-857, DOI: 10.1002/slct.201802608.
[22] A. Maleki, One-pot three-component synthesis of pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolines using Fe3O4@SiO2–OSO3H as an efficient heterogeneous nanocatalyst, RSC Advances, 4 (2014) 64169-64173, DOI: 10.1039/C4RA10856F.
[23] J. Zheng, Z.Q. Liu, X.S. Zhao, M. Liu, X. Liu, W. Chu, One-step solvothermal synthesis of Fe3O4@C core–shell nanoparticles with tunable sizes, Nanotechnology, 23 (2012) 165601, DOI: 10.1088/0957-4484/23/16/165601.
[24] M. Bystrzejewski, Synthesis of carbon-encapsulated iron nanoparticles via solid state reduction of iron oxide nanoparticles, Journal of Solid State Chemistry, 184 (2011) 1492-1498, DOI: 10.1016/j.jssc.2011.04.018.
[25] X.-W. Wei, G.-X. Zhu, C.-J. Xia, Y. Ye, A solution phase fabrication of magnetic nanoparticles encapsulated in carbon, Nanotechnology, 17 (2006) 4307, DOI: 10.1088/0957-4484/17/17/004.
[26] Z. Wang, P. Xiao, N. He, Synthesis and characteristics of carbon encapsulated magnetic nanoparticles produced by a hydrothermal reaction, Carbon, 44 (2006) 3277-3284, DOI: 10.1016/j.carbon.2006.06.026.
[27] H. Ghavidel, B. Mirza, S. Soleimani-Amiri, A Novel, Efficient, and Recoverable Basic Fe3O4@C Nano-Catalyst for Green Synthesis of 4H-Chromenes in Water via One-Pot Three Component Reactions, Polycyclic Aromatic Compounds, 41 (2021) 604-625, DOI: 10.1080/10406638.2019.1607413.
[28] H. Ghavidel, B. Mirza, S. Soleimani-Amiri, M. Manafi, New insight into experimental and theoretical mechanistic study on a green synthesis of functionalized 4H-chromenes using magnetic nanoparticle catalyst, Journal of the Chinese Chemical Society, 67 (2020) 1856-1876, DOI: 10.1002/jccs.201900554.
[29] M. Patil, S. Bagul, J. Rajput, R. Bendre, Clean Synthesis of Coumarin-3-Carboxylic Acids in Water Extract Rice (WERS), Green Materials, 6 (2018) 1-20, DOI: 10.1680/jgrma.18.00007.
[30] W.-Y. Pan, Y.-M. Xiao, H.-Q. Xiong, C.-W. Lü, Et3N catalyzed cascade reaction of Meldrum’s acid with ortho-hydroxyaryl aldehydes for the synthesis of coumarin-3-carboxylic acids under solvent-less condition, Research on Chemical Intermediates, 42 (2016) 7057-7063, DOI: 10.1007/s11164-016-2517-8.