How to cite this paper
Khdera, H. (2024). Design, synthesis and characterization of new azoflavone derivatives through diazotisation - coupling reactions of aromatic amines (sulfanilic acid, 2-amino pyridine).Current Chemistry Letters, 13(3), 477-482.
Refrences
1. Saunders, K. H., Allen R. L. M. (1985) Aromatic Diazo compounds, 3rd Ed, Edward Arnold Publishers, London.
2. Hunger, K. (2003) Industrial dyes: chemistry, properties, applications, Wiley, Weinheim.
3. Shankarling, G. S., Deshmukh, P. P., Joglekar, A. R. (2017) Process intensification in azo dyes, J Environ Chem Eng. 5, 3302-3308.
4. Zollinger, H. (1991) Color chemistry: syntheses, properties and application of organic dyes and pigments, 2nd Ed, John Wiley, New York.
5. Fadda, A. A., Etman, H. A., Amer, F. A., Barghout, M., Mohamed, Kh. S. (1994) Azo disperse dyes for synthetic fibres. I: 2-Methyl- and 2-phenylquinazolone derivative, J Chem Tech Biotechnol. 61343.
6. Liu, Z. F., Hashimoto, K., Fujishima, A. (1990) Photoelectrochemical information storage using an azobenzene derivative. Nature. 347, 658-660.
7. Negishi, M., Kanie, K., Ikeda, T., HIYAMA, T. (1996) Synthesis and Photochemical Switching of the Antiferroelectric Liquid Crystals Containing a Diazenediyl Group. Chem Lett. 8, 583-584.
8. Tanaka, K., Matsuo, K., Nakanishi, A., Jo, M., Shiota, H., Yamaguchi, M., Yoshino, S., Kawaguchi, K. (1984) syntheses and antimicrobial activities of five-membered heterocycles having a phenylazo substituent. Chem.Pharm. Bull. 32 (8), 3291-3298
9. Sharma, P., Rane, N., Gurram, V. K. (2004) Synthesis and QSAR studies of pyrimido[4,5-d]pyrimidine-2,5-dione derivatives as potential antimicrobial agents. Bioorg Med Chem. 14, 4185-4190.
10. Dias, M. C., Pinto, D. C. G. A., Silva, A. M. S. (2021) Plant Flavonoids: Chemical Characteristics and Biological Activity. Molecules. 26 (17), 5377.
11. Luna, R. De., Luisa, S., Ramírez-Garza, R. E. (2020) Environmentally Friendly Methods for Flavonoid Extraction from Plant Material: Impact of Their Operating Conditions on Yield and Antioxidant Properties. The Scientific World Journal. 6792069.
12. Hollman, P. C. H., Katan, M. B. (1999) Dietary Flavonoids: Intake, Health Effects and Bioavailability. Food and Chemical Toxicology. 37, 937-942.
13. Panche, A. N., Diwan, A. D., Chandra, S. R. (2016) Flavonoids: an overview. J Nutr Sci. 5, e47.
14. Zhang, M., Chen, X., Zhang, Y., Zhao, X., Zhao, J., Wang, X. (2022) The potential of functionalized dressing releasing flavonoids facilitates scar-free healing. Front Med (Lausanne). 3(9), 978120.
15. Rakha, A., Umar, N., Rabail, R., Sadiq, B. M., Kieliszek, M., Hassoun, A. , Aadil, R.M. (2022) Anti-inflammatory and anti-allergic potential of dietary flavonoids: A review, Biomedicine & Pharmacotherapy. 156, 113945.
16. Boniface, P. K., Ferreira, E. I. (2019) Flavonoids as efficient scaffolds: recent trends for malaria, leishmaniasis, chagas disease, and dengue. Phytotherapy Research. 33 (10), 2473-2517.
17. Huang, W., Wang, Y., Tian, W., Cui, X., Tu, P., Li, J., Shi, S., Liu, X. (2022) Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics. 11 (10), 1380.
18. Luo, Y., Jian, Y., Liu, Y., Jiang, S., Muhammad, D., Wang, W. (2022) Flavanols from Nature: A Phytochemistry and Biological Activity Review. Molecules. 27(3), 719.
19. Khdera, H. A., Saad, S. Y., Moustapha, A., Kandil, F. (2023) Design, synthesis and characterization of azo group-containing flavonoid derivatives. Arkivoc. (vii) 12010, 1-12.
20. Patil, V. C. (2012) Synthesis and in vitro antiplaque activity of chalcone, flavonol and flavanol derivatives. IJPSR. 3(12), 5006-5014.
2. Hunger, K. (2003) Industrial dyes: chemistry, properties, applications, Wiley, Weinheim.
3. Shankarling, G. S., Deshmukh, P. P., Joglekar, A. R. (2017) Process intensification in azo dyes, J Environ Chem Eng. 5, 3302-3308.
4. Zollinger, H. (1991) Color chemistry: syntheses, properties and application of organic dyes and pigments, 2nd Ed, John Wiley, New York.
5. Fadda, A. A., Etman, H. A., Amer, F. A., Barghout, M., Mohamed, Kh. S. (1994) Azo disperse dyes for synthetic fibres. I: 2-Methyl- and 2-phenylquinazolone derivative, J Chem Tech Biotechnol. 61343.
6. Liu, Z. F., Hashimoto, K., Fujishima, A. (1990) Photoelectrochemical information storage using an azobenzene derivative. Nature. 347, 658-660.
7. Negishi, M., Kanie, K., Ikeda, T., HIYAMA, T. (1996) Synthesis and Photochemical Switching of the Antiferroelectric Liquid Crystals Containing a Diazenediyl Group. Chem Lett. 8, 583-584.
8. Tanaka, K., Matsuo, K., Nakanishi, A., Jo, M., Shiota, H., Yamaguchi, M., Yoshino, S., Kawaguchi, K. (1984) syntheses and antimicrobial activities of five-membered heterocycles having a phenylazo substituent. Chem.Pharm. Bull. 32 (8), 3291-3298
9. Sharma, P., Rane, N., Gurram, V. K. (2004) Synthesis and QSAR studies of pyrimido[4,5-d]pyrimidine-2,5-dione derivatives as potential antimicrobial agents. Bioorg Med Chem. 14, 4185-4190.
10. Dias, M. C., Pinto, D. C. G. A., Silva, A. M. S. (2021) Plant Flavonoids: Chemical Characteristics and Biological Activity. Molecules. 26 (17), 5377.
11. Luna, R. De., Luisa, S., Ramírez-Garza, R. E. (2020) Environmentally Friendly Methods for Flavonoid Extraction from Plant Material: Impact of Their Operating Conditions on Yield and Antioxidant Properties. The Scientific World Journal. 6792069.
12. Hollman, P. C. H., Katan, M. B. (1999) Dietary Flavonoids: Intake, Health Effects and Bioavailability. Food and Chemical Toxicology. 37, 937-942.
13. Panche, A. N., Diwan, A. D., Chandra, S. R. (2016) Flavonoids: an overview. J Nutr Sci. 5, e47.
14. Zhang, M., Chen, X., Zhang, Y., Zhao, X., Zhao, J., Wang, X. (2022) The potential of functionalized dressing releasing flavonoids facilitates scar-free healing. Front Med (Lausanne). 3(9), 978120.
15. Rakha, A., Umar, N., Rabail, R., Sadiq, B. M., Kieliszek, M., Hassoun, A. , Aadil, R.M. (2022) Anti-inflammatory and anti-allergic potential of dietary flavonoids: A review, Biomedicine & Pharmacotherapy. 156, 113945.
16. Boniface, P. K., Ferreira, E. I. (2019) Flavonoids as efficient scaffolds: recent trends for malaria, leishmaniasis, chagas disease, and dengue. Phytotherapy Research. 33 (10), 2473-2517.
17. Huang, W., Wang, Y., Tian, W., Cui, X., Tu, P., Li, J., Shi, S., Liu, X. (2022) Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics. 11 (10), 1380.
18. Luo, Y., Jian, Y., Liu, Y., Jiang, S., Muhammad, D., Wang, W. (2022) Flavanols from Nature: A Phytochemistry and Biological Activity Review. Molecules. 27(3), 719.
19. Khdera, H. A., Saad, S. Y., Moustapha, A., Kandil, F. (2023) Design, synthesis and characterization of azo group-containing flavonoid derivatives. Arkivoc. (vii) 12010, 1-12.
20. Patil, V. C. (2012) Synthesis and in vitro antiplaque activity of chalcone, flavonol and flavanol derivatives. IJPSR. 3(12), 5006-5014.