References
- Zefirov, N. S.; Matveeva, E. D. Catalytic Kabachnik-Fields Reaction: New Horizons for Old Reaction. ARKIVOC 2008, 1, 1–17. DOI: https://doi.org/10.3998/ark.5550190.0009.101.
- Kafarski, P.; Lejczak, B. Aminophosphonic Acids of Potential Medical Importance. Curr. Med. Chem. Anticancer Agents. 2001, 1, 301–312. DOI: https://doi.org/10.2174/1568011013354543.
- Fields, S. C. Synthesis of Natural Products Containing a C-P Bond. Tetrahedron 1999, 55, 12237–12272. DOI: https://doi.org/10.1016/S0040-4020(99)00701-2.
- Menor-Salván, C.; Marín-Yaseli, M. R. Prebiotic Chemistry in Eutectic Solutions at the Water-Ice Matrix. Chem. Soc. Rev. 2012, 41, 5404–5415. DOI: https://doi.org/10.1039/C2CS35060B.
- Quin, L. D.; Tyrell, J. A. Fundamentals of Heterocyclic Chemistry: importance in Nature and in the Synthesis of Pharmaceuticals; John Wiley & Sons: Hoboken, NJ, 2010.
- Pozharskii, A. F.; Soldatenkov, A. T.; Katritzky, A. R. Heterocycles in Life and Society: An Introduction to Heterocyclic Chemistry, Biochemistry and Applications. John Wiley & Son: Hoboken, NJ, 2011.
- Onita, N.; Sisu, I.; Penescu, M.; Purcarea, V. L.; Kurunczi, L. Synthesis, Characterization and Biological Activity of Some α-Aminophosphonates. Farmacia 2010, 58, 531–545. DOI:/20105/issue52010art01-531-545.
- Chen, S.; Cowark, J. K. A General Method for the Synthesis of N-Protected α-Aminoalkylphosphinic Acids. Tetrahedron Lett. 1996, 37, 4335–4338. DOI: https://doi.org/10.1016/0040-4039(96)00839-8.
- Peyman, A.; Stahl, W.; Wagner, K.; Ruppert, D.; Budt, K. H. Human Immunodeficiency Virus-1 Protease. Bioorg. Med. Chem. Lett. 1994, 4, 2601–2604. DOI: https://doi.org/10.1016/S0960-894X(01)80292-4.
- Meng, F.; He, F.; Song, X.; Zhang, L.; Hu, W.; Liu, G.; J, X. Facile Synthesis of Hybrid Sulfonophosphinodipeptides Composing of Taurines and 1-Aminoalkylphosphinic Acids. Amino Acids. J. Med. Chem. 2012, 43, 423–429. DOI: https://doi.org/10.1007/s00726-011-1098-5.
- Krishnaa, A. B.; Reddya, M. V.; Reddya, G. C.; Krishnaa, B. S.; Nayakb, S. K.; Reddy, C. S. Synthesis, anti-Oxidant and Antibacterial Properties of Diethyl (4-Flouro-3-Nitro Phenylamino)(Substituted Phenyl) Methyl Phosphonates. Int. J. Appl. Biol. Pharm. 2010, 3, 873–882. DOI: 62018-%20Suresh%20reddy-SVU
- Wang, X.; Cai, Y.; Chen, J.; Verpoort, F. A Simple Protocol for the Synthesis of α-Substituted Phosphonates. Phosphorus Sulfur Silicon Relat. Elem. 2016, 191, 1268–1273. DOI: https://doi.org/10.1080/10426507.2016.1167056.
- Buys, J. The Development of Low Generation Cyclic-Cored Metallodendrimers for Potential Application in anti-Cancer Therapy. PhD Thesis, Stellenbosch University, 2017. DOI: scholar.sun.ac.za/handle/10019.1/102833.
- Ramana, K. V.; Rasheed, S.; Sekhar, K. C.; Adam, S.; Raju, C. N. One-Pot and Catalyst-Free Synthesis of Novel α-Aminophosphonates under Microwave Irradiation and Their Biological Activity. Der. Pharm. Lett. 2012, 2, 456–463. DOI: 62b844c1e9159b9322118852052c98481ee320e3.
- Keglevich, G.; Bálint, E. The Kabachnik–Fields Reaction: Mechanism and Synthetic Use. Molecules 2012, 17, 12821–12835. DOI: https://doi.org/10.3390/molecules171112821.
- Kabachnik, M. M.; Zobnina, E. V.; Beletskaya, I. P. Microwave-Assisted Reactions of Schiff Bases with Diethyl Phosphonate in the Presence of CdI2. Russ. J. Org. Chem. 2005, 41, 505–507. DOI: https://doi.org/10.1007/s11178-005-0194-y.
- Dindulkar, S. D.; Reddy, M. V.; Jeong, Y. T. Cd (ClO4) 2· xH2O as a Novel Catalyst for the Synthesis of α-Aminophosphonates Under Solvent-Free Conditions. Catal. Commun. 2012, 17, 114–117. DOI: https://doi.org/10.1016/j.catcom.2011.10.025.
- Yadav, J. S.; Wholey, M. H.; Kuntz, R. E.; Fayad, P.; Katzen, B. T.; Mishkel, G. J.; Bajwa, T. K.; Whitlow, P.; Strickman, N. E.; Jaff, M. R.; et al. Protected Carotid-Artery Stenting versus Endarterectomy in High-Risk Patients. N. Engl. J. Med. 2004, 351, 1493–1501. DOI: https://doi.org/10.1056/NEJMoa040127.
- Ghosh, R.; Maiti, S.; Chakraborty, A.; Maiti, D. K. In(OTf)3 Catalysed Simple One-Pot Synthesis of α-Amino Phosphonates. J. Mol. Catal. A Chem. 2004, 210, 53–57. DOI: https://doi.org/10.1016/j.molcata.2003.09.020.
- Chandrasekhar, S.; Prakash, S. J.; Jagadeshwar, V.; Narsihmulu, C. Three Component Coupling Catalyzed by TaCl5-SiO2: synthesis of α-Amino Phosphonates. Tetrahedron Lett. 2001, 42, 5561–5563. DOI: https://doi.org/10.1016/S0040-4039(01)01053-X.
- Karki, B. S.; Verma, S.; Agrwal, A.; Kasana, V. One Pot three component organocatalyzed synthesis of octahydroquinazolinones. Int. J. Chem. Stud. 2017, 5, 280–290. http://www.chemijournal.com/archives/?year=2017&vol=5&issue=2&ArticleId=452&si=false.
- Yadav, J. S.; Reddy, B. V.; Madan, C. Montmorillonite Clay-Catalyzed One-Pot Synthesis of α-Amino Phosphonates. Synlett 2001, 2001, 1131–1133. https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-2001-15162.pdf. DOI: https://doi.org/10.1055/s-2001-15162.
- To, W. K.; Fothergill, A. W.; Rinaldi, M. G. Comparative Evaluation of Macrodilution and Alamar Colorimetric Microdilution Broth Methods for Antifungal Susceptibility Testing of Yeast Isolates. J. Clin. Microbiol. 1995, 33, 2660–2664. https://jcm.asm.org/content/33/10/2660.short. DOI: https://doi.org/10.1128/JCM.33.10.2660-2664.1995.
- Beyth, N.; Houri-Haddad, Y.; Domb, A.; Khan, W.; Hazan, R. Alternative Antimicrobial Approach: nano-Antimicrobial Materials. Evid. Based Complem. Alternat. Med. 2015, 2015, 246012. https://www.hindawi.com/journals/ecam/2015/246012/ DOI: https://doi.org/10.1155/2015/246012.
- Choi, C. W.; Kim, S. C.; Hwang, S. S.; Choi, B. K.; Ahn, H. J.; Lee, M. Y.; Park, S. H.; Kim, S. K. Antioxidant Activity and Free Radical Scavenging Capacity between Korean Medicinal Plants and Flavonoids by Assay-Guided Comparison. Plant Sci. 2002, 163, 1161–1168. DOI: https://doi.org/10.1016/S0168-9452(02)00332-1.
- Murugesan, A.; Gengan, R. M.; Krishnan, A. Sulfonic Acid Functionalized Boron Nitride Nano Materials as a Microwave-Assisted Efficient and Highly Biologically Active One-Pot Synthesis of Piperazinyl-Quinolinyl Fused Benzo [c] Acridine Derivatives. Mater. Chem. Phys. 2017, 188, 154–167. DOI: https://doi.org/10.1016/j.matchemphys.2016.12.039.
- Murugesan, A.; Gengan, R. M.; Rajamanikandan, R.; Ilanchelian, M. One-Pot Synthesis via 1, 3-Dipolar Cycloaddition Reaction to Piperazinyl-Quinolinyl Dispiro Heterocyclic Derivatives and Spectrofluorometric and Molecular Docking Studies on Their Binding with Human Serum Albumin. J. Mol. Struct. 2017, 1149, 439–451. DOI: https://doi.org/10.1016/j.molstruc.2017.08.017.
- Murugesan, A.; Gengan, R. M.; Rajamanikandan, R.; Ilanchelian, M.; Lin, C. H. One-Pot Synthesis of Claisen–Schmidt Reaction through (E)-Chalcone Derivatives: Spectral Studies in Human Serum Albumin Protein Binding and Molecular Docking Investigation. Synth. Commun. 2017, 47, 1884–1904. DOI: https://doi.org/10.1080/00397911.2017.1355466.