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An Effective Synthesis of 3-Methoxyflavones via 1-(2-Hydroxyphenyl)-2-methoxy-3-phenyl-1,3-propanediones

  • Lee, Jae-In (Department of Chemistry and Plant Resources Research Institute, College of Natural Science, Duksung Women's University) ;
  • Park, Se-Bin (Department of Chemistry and Plant Resources Research Institute, College of Natural Science, Duksung Women's University)
  • Received : 2011.12.30
  • Accepted : 2012.01.13
  • Published : 2012.04.20

Abstract

Keywords

References

  1. Bohm, B. A. Introduction to Flavonoids; Harwood Academic Publishers: Amsterdam, Netherlands, 1998; p 5.
  2. Williams, C. A.; Grayer, R. J. Nat. Prod. Rep. 2004, 21, 539. https://doi.org/10.1039/b311404j
  3. Ponce, M. A.; Scervino, J. M.; Erra-Balsells, R.; Ocampo, J. A.; Godeas, A. M. Phytochem. 2004, 65, 1925. https://doi.org/10.1016/j.phytochem.2004.06.005
  4. Veitch, N. C.; Grayer, R. J. Nat. Prod. Rep. 2008, 25, 555. https://doi.org/10.1039/b718040n
  5. Lu, H. W.; Sugahara, K.; Sagara, Y.; Masuoka, N.; Asaka, Y.; Manabe, M.; Kodama, H. Arch. Biochem. and Biophy. 2001, 393, 73. https://doi.org/10.1006/abbi.2001.2457
  6. Al-Dabbas, M. M.; Kitahara, K.; Suganuma, T.; Hashimoto, F.; Tadera, K. Biosci. Biotechnol. Biochem. 2006, 70, 2178. https://doi.org/10.1271/bbb.60132
  7. Li, B.-L.; Yang, Z.-J.; Jiang, L.-L.; Zhang, X.-Q.; Gu, H.-M.; Wang, H.-C.; Tian, X.-H. Bull. Korean Chem. Soc. 2009, 30, 1459. https://doi.org/10.5012/bkcs.2009.30.7.1459
  8. Wang, H.-K.; Bastow, K. F.; Cosentino, L. M.; Lee, K.-H. J. Med. Chem. 1996, 39, 1975. https://doi.org/10.1021/jm960008c
  9. Diaz, F.; Chavez, D.; Lee, D.; Mi, Q.; Chai, H.-B.; Tan, G. T.; Kardono, L. B. S.; Riswan, S.; Fairchild, C. R.; Wild, R.; Farnsworth, N. R.; Cordell, G. A.; Pezzuto, J. M.; Kinghorn, A. D. J. Nat. Prod. 2003, 66, 865. https://doi.org/10.1021/np0300784
  10. Kim, J. Y.; Lim, H. J.; Ryu, J.-H. Bioorg. & Med. Chem. Lett. 2008, 18, 1511. https://doi.org/10.1016/j.bmcl.2007.12.052
  11. Abdel-Kader, M. S.; Alqasoumi, S. I.; Al-Taweel, A. M. Chem. Pharm. Bull. 2009, 57, 620. https://doi.org/10.1248/cpb.57.620
  12. Berti, G.; Livi, O.; Segnini, D.; Cavero, I. Tetrahedron 1967, 23, 2295. https://doi.org/10.1016/0040-4020(67)80066-8
  13. Li, J.-J. Name Reactions in Heterocyclic Chemistry; John Wiley & Sons: New Jersey, U. S. A., 2005; p 521.
  14. Daskiewicz, J.-B.; Depeint, F.; Viornery, L.; Bayet, C.; Comte-Sarrazin, G.; Comte, G.; Gee, J. M.; Johnson, I. T.; Ndjoko, K.; Hostettmann, K.; Barron, D. J. Med. Chem. 2005, 48, 2790. https://doi.org/10.1021/jm040770b
  15. Deng, B.-L.; Lepoivre, J. A.; Lemiere, G.; Dommisse, R.; Claeys, M.; Boers, F.; Groot, A. D. Liebigs Ann. Recueil 1997, 2169.
  16. Bois, F.; Beney, C.; Mariotte, A.-M.; Boumendjel, A. Synlett 1999, 1480.
  17. Pandey, G.; Krishna, A.; Kumaraswamy, G. Tetrahedron Lett. 1987, 28, 4615. https://doi.org/10.1016/S0040-4039(00)96580-8
  18. Meyer, N. D.; Haemers, A.; Mishra, L.; Pandey, H.-K.; Pieters, L. A. C.; Berghe, D. A. V.; Vlietinck, A. J. J. Med. Chem. 1991, 34, 736. https://doi.org/10.1021/jm00106a039
  19. Fougerousse, A.; Gonzalez, E.; Brouillard, R. J. Org. Chem. 2000, 65, 583. https://doi.org/10.1021/jo990735q
  20. Horie, T.; Kawamura, Y.; Yamamoto, H.; Yamashita, K. Chem. Pharm. Bull. 1995, 43, 2054. https://doi.org/10.1248/cpb.43.2054
  21. Lee, J. I.; Son, H. S.; Park, H. Bull. Korean Chem. Soc. 2004, 25, 1945. https://doi.org/10.5012/bkcs.2004.25.12.1945
  22. Lee, J. I.; Son, H. S.; Jung, M. G. Bull. Korean Chem. Soc. 2005, 26, 1461. https://doi.org/10.5012/bkcs.2005.26.9.1461

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