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Eco-friendly and simple synthesis of some non-natural flavones through chalcones
Mohammad Saidur Rahman (1) , Sayeda Shakila Alam (2) , Kamrunnahar Happy (3) , Mohammad Mamun Hossain (4) , Mohammad Khademul Islam (5,*) , Foni Bushon Biswas (6)
(1) Department of Chemistry, Faculty of Mathematical and Physical Sciences, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
(2) Department of Chemistry, Faculty of Mathematical and Physical Sciences, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
(3) Department of Chemistry, Faculty of Mathematical and Physical Sciences, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
(4) Department of Chemistry, Faculty of Mathematical and Physical Sciences, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
(5) Department of Chemistry, Faculty of Science, Mawlana Bhashani Science and Technology University, Santosh, Tangail-1902, Bangladesh
(6) Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong-4331, Bangladesh
(*) Corresponding Author
Received: 08 May 2018 | Revised: 04 Jun 2018 | Accepted: 06 Jun 2018 | Published: 30 Sep 2018 | Issue Date: September 2018
A distinctive feature of polyphenolics is the possession of biological properties such as antioxidant and antimicrobial activities. Simple synthesis and study about such important class of compounds and their analogs are very important to enhance the understanding of their role in human health and diseases. Accordingly, a series of chalcones (2a-f) have been synthesized by Claisen-Schmidt condensation reaction with required acetophenones and aromatic aldehydes in high yields. The conversion of chalcones to the corresponding flavones (1a-g) taking minimal amount of dimethyl sulfoxide with iodine in presence of sulfuric acid was carried out under microwave conditions in high yields.
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The Ministry of Science and Technology, Government of the People’s Republic of Bangladesh.
. Tahara, S.; Ingham, J. L.; Nakahara, S.; Mizutani, J.; Harborne, J. B. Phytochemistry 1984, 23(9), 1889-1900.
. Brown, J. P. Mutat. Res. Rev. Genet. Tox. 1980, 75(3), 243-277.
. Mabry, T. J.; Harborne, J. B. The Flavonoids: Advances in Research, Chapman and Hall: London, 1982, pp. 535.
. Hollman, P. C. H.; Katan, M. B. Food Chem. Toxicol. 1999, 37(9), 937-942.
. Learmonth, D. A. Synth. Commun. 2002, 32(18), 2757-2762.
. Sahu, S. C.; Gray, G. C. Cancer Lett. 1996, 104(2), 193-196.
. Cushnie, T. P. T.; Lamb, A. J. Int. J. Antimicrob. Agents 2005, 26(5), 343-356.
. O'Prey, J.; Brown, J.; Fleming, J.; Harrison, P. R. Biochem. Pharmacol. 2003, 66(11), 2075-2088.
. Ren, W.; Qiao, Z.; Wang, H.; Zhu, L.; Zhang, L. Med. Res. Rev. 2003, 23(4), 519-534.
. Cermak, R.; Wolffram, S. Curr. Drug Metab. 2006, 7(7), 729-744.
. Machida, K.; Osawa, K. Chem. Pharm. Bull. 1989, 37(4), 1092-1094.
. Ullmannova, V.; Popescu, N. C. Cancer Detect. Prev. 2007, 31 (2), 110-118.
. Ruffmann, R. J. Int. Med. Res. 1988, 16(5), 317-330.
. Hossain, M. M.; Kawamura, Y.; Yamashita, K.; Tsukayama, M. Tetrahedron 2006, 62(36), 8625-8635.
. Strauss, C. R.; Trainor, R. W. Aust. J. Chem. 1995, 48(10), 1665-1692.
. Giguere, R. J.; Bray, T. L.; Duncan, S. M.; Majetich, G. Tetrahedron Lett. 1986, 27(41), 4945-4948.
. Varma, R. S. Green Chem. 1999, 1(1), 43-55.
. Hachiya, I.; Moriwaki, M.; Kobayashi, S. Bull. Chem. Soc. Jpn. 1995, 68(7), 2053-2060.
. Olah, G. A. Friedel-crafts chemistry. World Scientific, 1973.
. Matsushita, Y.; Sugamoto, K.; Matsui, T. Tetrahedron Lett. 2004, 45(24), 4723-4727.
. Tsukayama, M.; Kusunoki, E.; Hossain, M. M.; Kawamura, Y.; Hayashi, S. Heterocycles 2007, 71(7), 1589-1600.
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DOI Link: https://doi.org/10.5155/eurjchem.9.3.236-240.1732
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