How to cite this paper
Dhaduk, M & Joshi, H. (2022). Synthesis, characterization and antimicrobial activity of some new isoxazole derivatives.Current Chemistry Letters, 11(3), 255-262.
Refrences
1. David A. Warrell, (2020) Hunter's Tropical Medicine and Emerging Infectious Diseases, Tenth Edition, pp.1006-1020.
2. Jesse P. W. and Richard C. L., (2007) The Synthesis of Highly Substituted Isoxazoles by Electrophilic Cyclization: An Efficient Synthesis of Valdecoxib, J. Org. Chem,, 72, 25, 9643–9647.
3. Abdel‐Hafiz S. A. and El‐Kholy Y. M., (1995) Heterocyclic dye synthesis: Synthesis and dye performance of new polyfunctionally isoxazole azo dye, Pigment and Resin Technology, 24 (5), 13-16.
4. Ki-Liang G., Zhao L. and Ze-Whi W., (2020) Design, Synthesis and Bioevaluation of Substituted Phenyl Isoxazole Analogs as Herbicide Safeners, Journal of Agricultural and Food Chemistry, 68 (39) 10550–10559.
5. Shin J. H., Gadde K. M., Ostbye T., Bray G. A., (2014) Weight changes in obese adults 6-months after discontinuation of double-blind Zonisamide or placebo treatment, Diabetes Obes Metab 16, 766–768.
6. Lainson J. C., Daly S. M., Triplett K., Johnston S. A., Hall P. R., Diehnelt C. W., (2017) Synthetic antibacterial peptide exhibits synergy with Oxacillin against MRSA. ACS Med Chem Lett, 8, 853–857.
7. Schoretsanitis G., Spina E., Hiemke C., De Leon J., (2017) A systematic review and combined analysis of therapeutic drug monitoring studies for long-acting risperidone, Expert Rev Clin Pharmacol, 10, 965–981.
8. Conti P., Roda G., Stabile H., Vanoni M. A., Curti B., De Amici M., (2003) Synthesis and biological evaluation of new amino acids structurally related to the antitumor agent Acivicin, Farmaco, 58, 683–690.
9. Golicki D., Newada M., Lis J., Pol K., Hermanowski T., Tłustochowicz M., (2012) Leflunomide in monotherapy of rheumatoid arthritis: meta-analysis of randomized trials, Pol Arch Med Wewn, 122, 22–32.
10. Shader R. I., Greenblatt D. J., (1999) The reappearance of a monamine oxidase inhibitor (Isocarboxazid), J Clin Psychopharmacol, 19, 105–106.
11. Karthikeyan K., Veenus Seelan T., Lalitha K. G., Perumal P. T., (2009) Synthesis and antinociceptive activity of pyrazolyl isoxazolines and pyrazolyl isoxazoles, Bioorg Med Chem Lett., 19, 3370–3373.
12. Rajanarendar E., Rama Krishna S., Nagaraju D., Govardhan Reddy K., Kishore B., Reddy Y. N., (2015) Environmentally benign synthesis, molecular properties prediction and anti-inflammatory activity of novel isoxazolo[5,4-d]isoxazol-3-yl-aryl-methanones via vinylogous Henry nitroaldol adducts as synthons, Bioorg Med Chem Lett, 25, 1630–1634.
13. Tzanetou E., Liekens S., Kasiotis K. M., Melagraki G., Afantitis A., Fokialakis N., Haroutounian S. A., (2014) Antiproliferative novel isoxazoles: Modeling, virtual screening, synthesis, and bioactivity evaluation, Eur J Med Chem., 81, 139–149.
14. Basha S. S., Divya K., Padmaja A., Padmavathi V., (2015) Synthesis and antimicrobial activity of thiazolyl pyrazoles and isoxazoles, Res Chem Intermed, 41, 10067–10083.
15. Lee Y. S., Park S. M., Kim B. H., (2009) Synthesis of 5-isoxazol-5-yl-2′- deoxyuridines exhibiting antiviral activity against HSV and several RNA viruses, Bioorg Med Chem Lett., 19, 1126–1128.
16. Page L. W., Bailey M., Beswick P. J., Frydrych S., Gleave R. J., (2010) The acid-mediated intramolecular 1, 3-dipolar cycloaddition of derived 2-nitro-1, 1-ethenediamines for the synthesis of novel fused bicyclic isoxazoles, Tetrahedron Lett., 51, 3388–3391.
17. Lasri J., Mukhopadhyay S., Charmier MAJ., (2008) Efficient regioselective synthesis of 4- and 5-substituted isoxazoles under thermal and microwave conditions, J Heterocycl Chem., 45, 1385–1389.
18. Buron C., El Kaim L., Uslu A., (1997) A new straightforward formation of aminoisoxazoles from isocyanides, Tetrahedron Lett., 38, 8027–8030.
19. Agrawal N. and Mishra P., (2018) The synthetic and therapeutic expedition of isoxazole and its analogs, Medicinal Chemistry Research, 27, 1309–1344.
20. Zawadzinska K., Ríos-Gutierrez M., Kula K., Wolinski P., Miroslaw B., Krawczyk T. and Jasinski R., (2021) The participation of 3,3,3-trichloro-1-nitroprop-1-ene in the [3+2] cycloaddition reaction with selected nitrile N-oxides in the light of the experimental and MEDT quantum chemical study, Molecules, 26, 6774.
21. Jasinski R. and Dresler E., (2020) Question of Zwitterionic Intermediates in the [3+2] Cycloaddition Reactions: A Critical Review, Organics, 1, 46-69.