Microwave assisted synthesis, characterization and biological activities of ferrocenyl chalcones and their QSAR analysis: Part II

References

• Dhar, D. N.; Dhar, D.; Barton, D. The Chemistry of Chalcones and Related Compounds; Wiley: New York, 1981.
   Google Scholar
• Shakil, N. A.; Singh, M. K.; Kumar, J.; Sathiyendiran, M.; Kumar, G.; Singh, M.; Pandey, R. P.; Pandey, A.; Parmar, V. S. Microwave Synthesis and Antifungal Evaluations of Some Chalcones and Their Derived Diaryl-Cyclohexenones. J. Environ. Sci. Health. B 2010, 45, 524–530. DOI: 10.1080/03601234.2010.493482.
   PubMed Web of Science ®Google Scholar
• Shakil, N. A.; Singh, M. K.; Sathiyendiran, M.; Kumar, J.; Padaria, J. C. Microwave Synthesis, Characterization and Bio-Efficacy Evaluation of Novel Chalcone Based 6-Carbethoxy-2-Cyclohexen-1-One and 2H-Indazol-3-ol Derivatives. Eur. J. Med. Chem. 2013, 59, 120–131. DOI: 10.1016/j.ejmech.2012.10.038.
   PubMed Web of Science ®Google Scholar
• Shakil, N. A.; Singh, M. K.; Sathiyendiran, M.; Kumar, J. Microwave Accelerated Solvent-Free Synthesis and Antifungal Evaluations of Flavanones. Arch. Phytopathol. Plant Protect. 2011, 44, 1958–1965. DOI: 10.1080/03235408.2010.544467.
   Google Scholar
• Vibhute, Y. B.; Baseer, M. A. Synthesis and Activity of a New Series of Chalcones as Antibacterial Agents. Indian. J. Chem. 2003, 42, 202–205.
   Google Scholar
• Alam, S. Synthesis, Antibacterial and Antifungal Activity of Some Derivatives of 2-Phenyl-Chromen-4-One. J. Chem. Sci. 2004, 116, 325–331. DOI: 10.1007/BF02711433.
   Web of Science ®Google Scholar
• Bag, S.; Ramar, S.; Degani, M. S. Synthesis and Biological Evaluation of α, β-Unsaturated Ketone as Potential Antifungal Agents. Med. Chem. Res. 2009, 18, 309–316. DOI: 10.1007/s00044-008-9128-x.
   Web of Science ®Google Scholar
• Kalirajan, R.; Sivakumar, S. U.; Jubie, S.; Gowramma, B.; Suresh, B. Synthesis and Biological Evaluation of Some Heterocyclic Derivatives of Chalcones. Int. J. Chemtech. Res. 2009, 1, 27–34.
   Google Scholar
• Caboni, P.; Aissani, N.; Demurtas, M.; Ntalli, N.; Onnis, V. Nematicidal Activity of Acetophenones and Chalcones against Meloidogyne incognita and Structure-Activity Considerations. Pest Manag. Sci. 2016, 72, 125–130. DOI: 10.1002/ps.3978.
   PubMed Web of Science ®Google Scholar
• Nolte, N. M.; Salmain, M. The Bioorganometallic Chemistry of Ferrocene. In Ferrocenes Ligands, Materials and Biomolecules; Stepnicka, P., Ed.; Wiley: West Sussex, 2008; pp 499–639.
   Google Scholar
• Wu, X.; Wilairat, P.; Go, M. L. Antimalarial Activity of Ferrocenyl Chalcones. Bioorg. Med. Chem. Lett. 2002, 12, 2299–2302. DOI: 10.1016/S0960-894X(02)00430-4.
   PubMed Web of Science ®Google Scholar
• Yadav, D. K.; Kaushik, P.; Pankaj, P.; Rana, V. S.; Kamil, D.; Khatri, D.; Shakil, N. A. Microwave Assisted Synthesis, Characterization and Biological Activities of Ferrocenyl Chalcones and Their QSAR Analysis. Front. Chem. 2019, 7, 814–829. DOI:10.3389/fchem.2019.00814.
   PubMed Web of Science ®Google Scholar
• Nene, Y. L.; Thapliyal, P. N. Fungicides in Plant Disease Control. In Evaluation of Fungicides; Nene, Y. L., Thapliyal, P. N., Eds.; Oxford and IBH Publishing Co.: New Delhi, 1979; pp 406–428.
   Google Scholar
• Abbott, W. S. A Methodology of Computing the Effectiveness of an Insecticide. J. Econ. Entomol. 1925, 18, 265–267. DOI: 10.1093/jee/18.2.265a.
   Web of Science ®Google Scholar
• Solcaniova, E.; Toma, S.; Fiedlerova, A. Investigation of Substituent Effects on the 1H and 13C NMR Spectra of Ferrocene Analogues of Chalcones. Org. Magn. Reson. 1980, 14, 181–185. DOI:10.1002/mrc.1270140307.
   Web of Science ®Google Scholar
• Golbraikh, A.; Tropsha, A. Beware of q2! J. Mol. Graph. Model. 2002, 20, 269–276. DOI: 10.1016/s1093-3263(01)00123-1.
   PubMed Web of Science ®Google Scholar
• Doweyko, A. M. 3D-QSAR Illusions. J. Comput. Aided Mol. Des. 2004, 18, 587–596. DOI: 10.1007/s10822-004-4068-0.
   PubMed Web of Science ®Google Scholar
• Ponce, Y.; Garit, J.; Torrens, F.; Zaldivar, V.; Castro, E. Atom, Atom-Type, and Total Linear Indices of the "Molecular Pseudograph's Atom Adjacency Matrix": Application to QSPR/QSAR Studies of Organic Compounds. Molecules 2004, 9, 1100–1123. DOI: 10.3390/91201100.
   PubMed Web of Science ®Google Scholar
• Kaushik, P.; Sarkar, D. J.; Chander, S.; Rana, V. S.; Shakil, N. A. Insecticidal Activity of Phenolic Acid Amides against Brown Planthopper (BPH), Nilaparvata Lugens (Stål) and their QSAR Analysis. J. Environ. Sci. Health. B 2019, 54, 489–497. DOI: 10.1080/03601234.2019.1574174.
   PubMed Web of Science ®Google Scholar
• Balaban, A. T. Highly Discriminating Distance-Based Topological Index. Chem. Phys. Lett. 1982, 89, 399–404. DOI: 10.1016/0009-2614(82)80009-2.
   Web of Science ®Google Scholar