References
- Popiołek, L. The Bioactivity of Benzenesulfonyl Hydrazones: A Short Review. Biomed. Pharmacother. 2021, 141, 111851. DOI: https://doi.org/10.1016/j.biopha.2021.111851.
- Somashekar, M. N.; Chetana, P. R. A Review on Anthracene and Its Derivatives: Applications. Res. Rev. J. Chem. 2016, 5, 45.
- Mukerjee, A. K. Azlactones: Retrospect and Prospect. Heterocycles 1987, 26, 1077. DOI: https://doi.org/10.3987/R-1987-04-1077.
- Khan, K. M.; Mughal, U. R.; Khan, M. T. H.; Ullah, Z.; Perveen, S.; Choudhary, M. I. Oxazolones: New Tyrosinase Inhibitors; Synthesis and Their Structure–Activity Relationships. Bioorg. Med. Chem. 2006, 14, 6027. DOI: https://doi.org/10.1016/j.bmc.2006.05.014.
- Kitazawa, M.; Higuchi, R.; Takahashi, M.; Wada, T.; Sasabe, H. Novel Molecular Design for Second-Harmonic Generation: Azlactone Derivatives. J. Phys. Chem. 1995, 99, 14784–14792. DOI: https://doi.org/10.1021/j100040a031.
- Youssef, A. S.; Kandeel, K. A.; Abou‐Elmagd, W. S.; Haneen, D. S. Action of Some Nitrogen and Carbon Nucleophile on 4-Arylidene-1,3-Oxazolones. J. Heterocyclic Chem. 2016, 53, 175–182. DOI: https://doi.org/10.1002/jhet.2411.
- Youssef, A. S.; Kandeel, K. A.; Abou‐Elmagd, W. S.; Haneen, D. S. Synthesis of Novel Heterocycles Derived from 4-Arylmethylene-2-Phenyl-1,3-Oxazole-5(4H)-Ones. J. Heterocyclic Chem. 2016, 53, 809–816. DOI: https://doi.org/10.1002/jhet.2329.
- Fisk, J. S.; Mosey, R. A.; Tepe, J. J. The Diverse Chemistry of Oxazol-5-(4H)-Ones. Chem. Soc. Rev. 2007, 36, 1432–1440. DOI: https://doi.org/10.1039/b511113g.
- Haneen, D. S.; Gouhar, R. S.; Hashem, H. E.; Youssef, A. S. Synthesis and Reactions of 4H-3,1-Benzoxazin-4-One Derivative Bearing Pyrazolyl Moiety as Antimicrobial and Antioxidant Agents. Synth. Commun. 2019, 49, 2840.
- Muthuboopathi, G.; Shanmugarajan, T. S. Synthesis, Characterization, and Biological Evaluation of Oxazolone Analogs. Asian J. Pharm. Clin. Res. 2018, 11, 159.
- Descas, P.; Panconi, E.; Jarry, C. Eur Pat Appl 1990, 392, 929, 17 Oct. Chem. Abstr. 1991, 114, 783.
- Benedlt, D.; Daniel, V. Synthesis of 2-Methyl-(Z)-4- (Phenylimino)Naphth[2,3-d]Oxazol-9-One, a Monoimine Quinone with Selective Cytotoxicity toward Cancer Cells. J. Med. Chem. 1994, 37, 710.
- Jat, L. R.; Mishra, R.; Pathak, D. Synthesis and Anticancer Activity of 4-Benzylidene-2-Phenyloxazol-5 (4H)-One Derivatives. Int. J. Pharm. Pharm. Sci. 2012, 4, 378.
- Viti, G.; Nannicini, R.; Ricci, R.; Pestellini, V.; Abelli, L.; Furio, M. New Antagonists of Platelet-Activating Factor Containing 2-Oxazolidinone or 2-Morpholinone. Eur. J. Med. Chem. 1994, 29, 401–406. DOI: https://doi.org/10.1016/0223-5234(94)90066-3.
- Pasha, M. A.; Jayashanka, V. P.; Venugopala, K. N.; Rao, G. K. Zinc Oxide (ZnO): An Efficient Catalyst for the Synthesis of 4-Arylmethylidene-2-Phenyl-5-(4H)-Oxazolones Having Antimicrobial Activity. J. Pharmacol. Toxicol. 2007, 2, 264–270. DOI: https://doi.org/10.3923/jpt.2007.264.270.
- Bala, S.; Saini, M.; Kamboj, S.; Saini, V. Synthesis of 2-[4-(Substituted Benzylidene)-5-Oxo-4, 5-Dihydro-Oxazol-2-Ylmethyl]-Isoindole-1, 3-Dione Derivatives as Novel Potential Antimicrobial Agents. Iran. J. Pharmacol. Ther. 2012, 11, 45.
- Mariappan, G.; Saha, B. P.; Datta, S.; Kumar, D.; Haldar, P. K. Design, Synthesis and Antidiabetic Evaluation of Oxazolone Derivatives. J. Chem. Sci. 2011, 123, 335–341. DOI: https://doi.org/10.1007/s12039-011-0079-2.
- Abdel-Aty, A. S. Pesticidal Effects of Some Imidazolidine and Oxazolone Derivatives. World J. Agric. Sci. 2009, 5, 105.
- Parveen, M.; Ali, A.; Ahmed, S.; Malla, A. M.; Alam, M.; Pereira Silva, P. S.; Silva, M. R.; Lee, D.-U. Synthesis, Bioassay, Crystal Structure and Ab Initio Studies of Erlenmeyer Azlactones. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2013, 104, 538–545. DOI: https://doi.org/10.1016/j.saa.2012.11.054.
- Haneen, D. S.; Abou-Elmagd, W. S.; Youssef, A. S. A.; 5(4H)-Oxazolones: Synthesis and Biological Activities. Synth. Commun. 2021, 51, 215–233. DOI: https://doi.org/10.1080/00397911.2020.1825746.
- Smokal, V.; Kolendo, A.; Krupka, O.; Sahraoui, B. Synthesis, Photophysical and Photochemical Properties of Oxazolone Derivatives. J. Optoel. Adv. Mater. 2008, 10, 607.
- Abou-Elregal, M. K.; Youssef, A. S. A.; Hemdan, M. M.; Samir, S. S. Reactivity of Z- and E-Isomers of 2-Benzamido-3-Phenylacrylohydrazide towards Some Carbon Electrophiles. A Comparative Study. Synth. Commun. 2019, 49, 2369–2378. DOI: https://doi.org/10.1080/00397911.2019.1623258.
- Abou-Elregal, M. K.; Mohamed, A. T. A.; Youssef, A. S. A.; Hemdan, M. M.; Samir, S. S.; Abou-Elmagd, W. S. I. Synthesis and Antitumor Activity Evaluation of Some 1,2, 4-Triazine and Fused Triazine Derivatives. Synth. Commun. 2018, 48, 2347–2357. DOI: https://doi.org/10.1080/00397911.2018.1482350.
- 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.
- Song, Z.; Chen, C. P.; Liu, J.; Wen, X.; Sun, H.; Yuan, H. Design, Synthesis, and Biological Evaluation of (2E)-(2-Oxo-1, 2-Dihydro-3H-Indol-3-Ylidene) Acetate Derivatives as anti-Proliferative Agents through ROS-Induced Cell Apoptosis. Eur. J. Med. Chem. 2016, 124, 809–819. DOI: https://doi.org/10.1016/j.ejmech.2016.09.005.
- Chander, S.; Tang, C. R.; Penta, A.; Wang, P.; Bhagwat, D. P.; Vanthuyne, N.; Albalat, M.; Patel, P.; Sankpal, S.; Zheng, Y. T.; Sankaranarayanan, M. Hit Optimization Studies of 3-Hydroxy-Indolin-2-One Analogs as Potential anti-HIV-1 Agents. Bioorg. Chem. 2018, 79, 212–222. DOI: https://doi.org/10.1016/j.bioorg.2018.04.027.
- Khetmalis, Y. M.; Shivani, M.; Murugesan, S.; Sekhar, K. V. G. C. Oxindole and Its Derivatives: A Review on Recent Progress in Biological Activities. Biomed. Pharmacother. 2021, 141, 111842. DOI: https://doi.org/10.1016/j.biopha.2021.111842.
- El‐Gohary, N. S.; Shaaban, M. I. Synthesis, Antimicrobial, Antiquorum-Sensing, and Cytotoxic Activities of New Series of Isoindoline-1,3-Dione, Pyrazolo[5,1-a]-Isoindole, and Pyridine Derivatives. Arch. Pharm. Chem. Life Sci. 2015, 348, 666–680. DOI: https://doi.org/10.1002/ardp.201500037.
- Abu-Hashem, A. A.; Gouda, M. A. Synthesis, anti-Inflammatory and Analgesic Evaluation of Certain New 3a,4,9,9a-Tetrahydro-4,9-Benzenobenz[f]Isoindole-1,3-Diones. Arch. Pharm. Pharm. Med. Chem. 2011, 344, 543–551. DOI: https://doi.org/10.1002/ardp.201100020.
- Vaidya, A.; Jain, S.; Jain, P.; Jain, P.; Tiwari, N.; Jain, R.; Jain, R.; Jain, A. K.; Agrawal, R. K. Synthesis and Biological Activities of Oxadiazole Derivatives: A Review. Mini Rev. Med. Chem. 2016, 16, 825–845. DOI: https://doi.org/10.2174/1389557516666160211120835.
- Ma, S.; Jiang, W.; Li, Q.; Li, T.; Wu, W.; Bai, H.; Shi, B. Design, Synthesis, and Study of the Insecticidal Activity of Novel Steroidal 1,3,4-Oxadiazoles. J. Agric. Food Chem. 2021, 69, 11572–11581. DOI: https://doi.org/10.1021/acs.jafc.1c00088.
- Sun, J.; Makawana, J. A.; Zhu, H. L. 1,3,4-Oxadiazole Derivatives as Potential Biological Agents. Mini Rev. Med. Chem. 2013, 13, 1725–1743. DOI: https://doi.org/10.2174/13895575113139990071.
- Verma, A.; Joshi, S.; Singh, D. Imidazole: Having Versatile Biological Activities. J. Chem. 2013, 2013, 1–12. DOI: https://doi.org/10.1155/2013/329412.
- Shalini, K.; Sharma, P. K.; Kumar, N. Imidazole and Its Biological Activities: A Review. Der. Chemica. Sinica. 2010, 1, 36.
- 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. 2012, 36, 75–82. DOI: https://doi.org/10.3184/174751912X13274297624330.
- 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. DOI: https://doi.org/10.1002/cjoc.201180264.
- Fieser, L. F.; Hartwell, J. L.; Jones, J. E.; Wood, J. H.; Bost, R. W. 9-Anthraldehyde. 2-Ethoxy-1-Naphthaldehyde. Org. Synth. 1940, 20, 11.
- Fawzy, N.; Ghobashy, M. O. I.; El-Ziaty, A. K. Synthesis and Antimicrobial Evaluation of Some New Quinazolin-4 (3H)-One Derivatives. Eur. J. Chem. 2012, 3, 437–441. DOI: https://doi.org/10.5155/eurjchem.3.4.437-441.677.
- Zhao, P.-L.; Wang, F.; Zhang, M.-Z.; Liu, Z.-M.; Huang, W.; Yang, G.-F. Synthesis, Fungicidal, and Insecticidal Activities of β-Methoxyacrylate-Containing N-Acetyl Pyrazoline Derivatives. J. Agric. Food Chem. 2008, 56, 10767–10773. DOI: https://doi.org/10.1021/jf802343p.
- Xu, R.; Xia, R.; Luo, M.; Xu, X.; Cheng, J.; Shao, X.; Li, Z. Design, Synthesis, Crystal Structures, and Insecticidal Activities of Eight-Membered Azabridge Neonicotinoid Analogues. J. Agric. Food Chem. 2014, 62, 381–390. DOI: https://doi.org/10.1021/jf4046683.