References
- Musa, M. A.; Cooperwood, J. S.; Omar, M.; Khan, F. A Review of Coumarin Derivatives in Pharmacotherapy of Breast Cancer. Curr. Med. Chem. 2008, 15, 2664–2679. DOI: https://doi.org/10.2174/092986708786242877.
- Arora, R. K.; Kaur, N.; Bansal, Y.; Bansal, G. Novel Coumarin-Benzimidazole Derivatives as Antioxidants and Safer Anti-inflammatory Agents. Acta Pharm. Sin. B. 2014, 4, 368–375. DOI: https://doi.org/10.1016/j.apsb.2014.07.001.
- Bansal, Y.; Sethi, P.; Bansal, G. Coumarin: A Potential Nucleus for anti-Inflammatory Molecules. Med. Chem. Res. 2013, 22, 3049–3060. DOI: https://doi.org/10.1007/s00044-012-0321-6.
- Nagamallu, R.; Kariyappa, A. K. Synthesis and Biological Evaluation of Novel Formylpyrazoles Bearing Coumarin Moiety as Potent Antimicrobial and Antioxidant Agents. Bioorg. Med. Chem. Lett. 2013, 23, 6406–6409.
- Bigi, F.; Chesini, L.; Maggi, R.; Sartori, G. Montmorillonite KSF as an Inorganic, Waterstable, and Reusable Catalyst for Knoevenagel Synthesis of Coumarin-3-Carboxylic Acids. J. Org. Chem. 1999, 64, 1033–1035. DOI: https://doi.org/10.1021/jo981794r.
- Al-Amiery, A. A.; Kadhum, A. A. H.; Mohamad, A. B. Antifungal Activities of New Coumarins. Molecules 2012, 17, 5713–5723. DOI: https://doi.org/10.3390/molecules17055713.
- Weigt, S.; Huebler, N.; Strecker, R.; Braunbeck, T.; Broschard, T. H. Developmental Effects of Coumarin and the Anticoagulant Coumarin Derivative Warfarin on Zebrafish (Danio rerio) Embryos. Reprod. Toxicol. 2012, 33, 133–141. DOI: https://doi.org/10.1016/j.reprotox.2011.07.001.
- Dey, S.; Lo, H. J.; Wong, C. H. An Efficient Modular One-Pot Synthesis of Heparin-Based Anticoagulant Idraparinux. J. Am. Chem. Soc. 2019, 141, 10309–10314. DOI: https://doi.org/10.1021/jacs.9b03266.
- Dey, S.; Lo, H. J.; Wong, C. H. Programmable One-Pot Synthesis of Heparin Pentasaccharide Fondaparinux. Org. Lett. 2020, 22, 4638–4642. DOI: https://doi.org/10.1021/acs.orglett.0c01386.
- Gacche, R. N.; Jadhav, S. G. Antioxidant Activities and Cytotoxicity of Selected Coumarin Derivatives: Preliminary Results of Astructure-Activity Relationship Study Using Computational Tools. J. Exp. Clin. Med. 2012, 4, 165–169. DOI: https://doi.org/10.1016/j.jecm.2012.04.007.
- Kawate, T.; Iwase, N.; Shimizu, M.; Stanley, S. A.; Wellington, S.; Kazyanskaya, E.; Hung, D. T. Synthesis and Structure-Activity Relationships of Phenyl-substituted Coumarins with Anti-tubercular Activity that Target FadD32. Bioorg. Med. Chem. Lett. 2013, 23, 6052–6059. DOI: https://doi.org/10.1016/j.bmcl.2013.09.035.
- Vogl, S.; Zehl, M.; Picker, P.; Urban, E.; Wawrosch, C.; Reznicek, G.; Saukel, J.; Kopp, B. Identification and Quantification of Coumarins in Peucedanum ostruthium (L.) Koch by HPLC-DAD and HPLC-DAD-MS. J. Agric. Food Chem. 2011, 59, 4371–4377. DOI: https://doi.org/10.1021/jf104772x.
- Wei, Y.; Zhang, T.; Ito, Y. Preparative Isolation of Osthol and Xanthotoxol from Common Cnidium Fruit (Chinese Traditional Herb) Using Stepwise Elution by High-Speed Counter-Current Chromatography. J. Chromatogr. A. 2004, 1033, 373–377. DOI: https://doi.org/10.1016/j.chroma.2004.01.058.
- Shi, Z.; Wang, F.; Zhou, W.; Zhang, P.; Fan, Y. J. Application of Osthol Induces a Resistance Response against Powdery Mildew in Pumpkin Leaves. IJMS. 2007, 8, 1001–1012. DOI: https://doi.org/10.3390/i8091001.
- Holbrook, A. M.; Pereira, J. A.; Labiris, R.; McDonald, H.; Douketis, J. D.; Crowther, M.; Wells, P. S. Systematic Overview of Warfarin and Its Drug and Food Interactions. Arch. Intern. Med. 2005, 165, 1095–1106. DOI: https://doi.org/10.1001/archinte.165.10.1095.
- Cesar, J. M.; Avello, A. G.; Navarro, J. L.; Herraez, M. V. Aging and Oral Anticoagulant Therapy Using Acenocoumarol. Blood Coagul. Fibrinolysis. 2004, 15, 673–676. DOI: https://doi.org/10.1097/00001721-200412000-00007.
- Ufer, M. Comparative Pharmacokinetics of Vitamin K Antagonists: Warfarin, Phenprocoumon and Acenocoumarol. Clin. Pharmacokinet. 2005, 44, 1227–1246. DOI: https://doi.org/10.2165/00003088-200544120-00003.
- Guan, A. Y.; Liu, C. L.; Li, M.; Zhang, H.; Li, Z. N.; Li, Z. M. Design, Synthesis and Structure-Activity Relationship of Novel Coumarin Derivatives. Pest Manag. Sci. 2011, 67, 647–655. DOI: https://doi.org/10.1002/ps.2103.
- Liu, C.; Guan, A.; Yang, J.; Chai, B.; Li, M.; Li, H.; Yang, J.; Xie, Y. Efficient Approach to Discover Novel Agrochemical Candidates: Intermediate Derivatization Method. J. Agric. Food Chem. 2016, 64, 45–51. DOI: https://doi.org/10.1021/jf5054707.
- Guan, A.; Liu, C.; Yang, X.; Dekeyser, M. Application of the Intermediate Derivatization Approach in Agrochemical Discovery. Chem. Rev. 2014, 114, 7079–7107. DOI: https://doi.org/10.1021/cr4005605.
- Hekal, M. H.; Abu El-Azm, F. S. M. New Potential Antitumor Quinazolinones Derived from Dynamic 2-Undecyl Benzoxazinone: Synthesis and Cytotoxic Evaluation. Synth. Commun. 2018, 48, 2391–2402. DOI: https://doi.org/10.1080/00397911.2018.1490433.
- Hekal, M. H.; Abu El-Azm, F. S. M. Efficient MW-Assisted Synthesis of Some New Isoquinolinone Derivatives with In Vitro Antitumor Activity. J. Het. Chem. 2017, 54, 3056–3064. DOI: https://doi.org/10.1002/jhet.2916.
- Mahmoud, M. R.; Abou-Elmagd, W. S. I.; Derbala, H. A.; Hekal, M. H. Synthesis and Spectral Characterisation of Some Phthalazinone Derivatives. J. Chem. Res. (S) 2012, 36, 75–82. DOI: https://doi.org/10.3184/174751912X13274297624330.
- Mahmoud, M. R.; Abu El-Azm, F. S. M.; Ismail, M. F.; Hekal, M. H.; Ali, Y. M. Synthesis and Antitumor Evaluation of Novel Tetrahydrobenzo[4′,5′]Thieno[3′,2′:5,6]Pyrimido[1,2-b]Isoquinoline Derivatives. Synth. Commun. 2018, 48, 428–438. DOI: https://doi.org/10.1080/00397911.2017.1406520.
- Mahmoud, M. R.; El-Shahawi, M. M.; Abou-Elmagd, W. S. I.; Hekal, M. H. Novel Synthesis of Isoquinoline Derivatives Derived from (Z)-4-(1,3-Diphenylpyrazol-4-yl)Isochromene-1,3-Dione. Synth. Commun. 2015, 45, 1632–1641. DOI: https://doi.org/10.1080/00397911.2015.1030760.
- Hekal, M. H.; El-Naggar, A. M.; Abu El-Azm, F. S. M.; El-Sayed, W. M. Synthesis of New Oxadiazol-Phthalazinone Derivatives with anti-Proliferative Activity; Molecular Docking, Pro-Apoptotic, and Enzyme Inhibition Profile. RSC Adv. 2020, 10, 3675–3688. DOI: https://doi.org/10.1039/C9RA09016A.
- Hekal, M. H.; Abu El-Azm, F. S. M.; Atta-Allah, S. R. Ecofriendly and Highly Efficient Microwave-Induced Synthesis of Novel Quinazolinone-Undecyl Hybrids with In Vitro Antitumor Activity. Synth. Commun. 2019, 49, 2630–2641. DOI: https://doi.org/10.1080/00397911.2019.1637001.
- Mahmoud, M. R.; Abou-Elmagd, W. S. I.; Derbala, H. A.; Hekal, M. H. Novel Synthesis of Some Phthalazinone Derivatives. Chin. J. Chem. 2011, 29, 1446–1450. DOI: https://doi.org/10.1002/cjoc.201180264.
- Abdelgawad, N.; Ismail, M. F.; Hekal, M. H.; Marzouk, M. I. Design, Synthesis, and Evaluation of Some Novel Heterocycles Bearing Pyrazole Moiety as Potential Anticancer Agents. J. Heterocyclic Chem. 2019, 56, 1771–1779. DOI: https://doi.org/10.1002/jhet.3544.
- Ali, A. M.; Hekal, M. H. Convenient Synthesis and anti-Proliferative Activity of Some Benzochromenes and Chromenotriazolopyrimidines under Classical Methods and Phase Transfer Catalysis. Synth. Commun. 2019, 49, 3498–3509. DOI: https://doi.org/10.1080/00397911.2019.1675173.
- Abu El-Azm, F. S. M.; El-Shahawi, M. M.; Elgubbi, A. S.; Madkour, H. M. F. Design, Synthesis, anti-Proliferative Activity, and Molecular Docking Studies of Novel Benzo[f]Chromene, Chromeno [2,3-d]Pyrimidines and Chromenotriazolo[1,5-c]Pyrimidines. Synth. Commun. 2020, 50, 669–683. DOI: https://doi.org/10.1080/00397911.2019.1710850.
- Abu El-Azm, F. S. M.; El-Shahawi, M. M.; Elgubbi, A. S.; Madkour, H. M. F. Synthesis of New Benzo[f]Chromene-Based Heterocycles Targeting anti-Proliferative Activity. J. Iran. Chem. Soc. 2021, 18, 1081–1092. DOI: https://doi.org/10.1007/s13738-020-02092-w.
- Dey, S.; Wong, C.-H. Programmable One-Pot Synthesis of Heparin Pentasaccharides Enabling Access to Regiodefined Sulfate Derivatives. Chem. Sci. 2018, 9, 6685–6691. DOI: https://doi.org/10.1039/C8SC01743C.
- Cheng, C. W.; Zhou, Y.; Pan, W. H.; Dey, S.; Wu, C. Y.; Hsu, W. L.; Wong, C. H. Hierarchical and Programmable One-Pot Synthesis of Oligosaccharides. Nat. Commun. 2018, 9, 5202–5210. DOI: https://doi.org/10.1038/s41467-018-07618-8.
- Mehrabi, H.; Ashraf, F. N.; Karimi, R. R. One-Pot Three-Component Condensation of β-Naphthol with Arylaldehydes and Meldrum’s Acid: Synthesis of 1-Aryl-1,2-Dihydro-Benzo[f]Chromen-3-Ones. J. Chem. Res. 2017, 41, 250–252. DOI: https://doi.org/10.3184/174751917X14902201357374.
- Okasha, R.; Alblewi, F.; Afifi, T.; Naqvi, A.; Fouda, A.; Al-Dies, A.-A.; El-Agrody, A. Design of New Benzo[h]Chromene Derivatives: Antitumor Activities and Structure-Activity Relationships of the 2,3-Positions and Fused Rings at the 2,3-Positions. Molecules 2017, 22, 479–496. DOI: https://doi.org/10.3390/molecules22030479.
- Salem, M. S.; Farhat, M.; Errayes, A. O.; Madkour, H. M. F. Antioxidant Activity of Novel Fused Heterocyclic Compounds Derived from Tetrahydropyrimidine Derivative. Chem. Pharm. Bull. 2015, 63, 866–872. DOI: https://doi.org/10.1248/cpb.c15-00452.
- Mkaouar, K.; Iriepa, I.; Iriepa, D. D.; Contelles, J. M.; Ismaili, L.; Chabchoub, F. Synthesis of (±)-Cis-1-Aryl-3-Oxo-2,3-Dihydro-1H-Benzo[f]Chromene-2-Carbonitriles and (±)-Trans-4-Aryl-2-Oxo-3,4-Dihydro-2H-Benzo[h]Chromene-3-Carbonitriles. Chem. Select 2019, 4, 12902–12905.
- Chaker, A.; Zribi, F.; Nepveu, F.; Chabchoub, F. Microwave Irradiation: Novel and Facile Methods for the Synthesis of New Pyrimidinones. Chin. Chem. Lett. 2014, 25, 1207–1210. DOI: https://doi.org/10.1016/j.cclet.2014.03.048.