DOI QR코드

DOI QR Code

Synthesis of 8-Triazolochrysin Analogs Through Click Reaction

  • Received : 2014.06.28
  • Accepted : 2014.08.07
  • Published : 2014.12.20

Abstract

Keywords

References

  1. Read, M. A. Am. J. Pathol. 1995, 147, 235.
  2. Harborne, J. B.; Williams, C. A. Phytochemistry 2000, 55, 481. https://doi.org/10.1016/S0031-9422(00)00235-1
  3. Hecker, M.; Preiss, C.; Klemm, P.; Brusse, R. Br. J. Pharmacol. 1996, 118, 2178. https://doi.org/10.1111/j.1476-5381.1996.tb15660.x
  4. Pearce, F. L.; Bienenstock, J. J. Allergy Clin. Immunol. 1984, 73, 819. https://doi.org/10.1016/0091-6749(84)90453-6
  5. Fishkin, R. J.; Winslow, J. T. Psychopharmacology (Berl.) 1997, 132, 335. https://doi.org/10.1007/s002130050353
  6. Habtemariam, S. J. Nat. Prod. 1997, 60, 775. https://doi.org/10.1021/np960581z
  7. Liang, Y. C.; Tsai, S. H.; Tsai, D. C.; Lin-Shiau, S. Y.; Lin, J. K. FEBS Lett. 2001, 496, 12. https://doi.org/10.1016/S0014-5793(01)02393-6
  8. Dao, T. T.; Kim, S. B.; Chi, Y. S.; Kim, H. P.; Sin, K.-S.; Park, H. Arch. Pharm. Res. 2003, 26, 581. https://doi.org/10.1007/BF02976703
  9. Dao, T. T.; Oh, J. W.; Sin, K.-S.; Kim, S.; Kim, H. P.; Park, H. Arch. Pharm. Res. 2004, 27, 278. https://doi.org/10.1007/BF02980059
  10. Park, H.; Dao, T. T.; Kim, H. P. Eur. J. Med. Chem. 2005, 40, 943. https://doi.org/10.1016/j.ejmech.2005.04.013
  11. Jang, J.; Sin, K.-S.; Kim, H. P.; Park, H. Yakhak Hoeji 2008, 52, 85.
  12. Park, H.; Dao, T. T.; Kim, H. P. Arch. Pharm. Res. Eur. 2009, 32, 1503. https://doi.org/10.1007/s12272-009-2101-5
  13. Che, H.; Lim, H.; Kim, H. P.; Park, H. Eur. J. Med. Chem. 2011, 46, 4657. https://doi.org/10.1016/j.ejmech.2011.04.044
  14. Lim, H.; Jin, J. H.; Park, H.; Kim, H. P. Eur. J. Pharmcol. 2011, 670, 617. https://doi.org/10.1016/j.ejphar.2011.09.010
  15. Su, N. N.; Li, Y.; Yu, S. J.; Zhang, X.; Liu, X. H.; Zhao, W. G. Res. Chem. Intermediat. 2013, 39, 759. https://doi.org/10.1007/s11164-012-0595-9
  16. Perera, D.; Fernandes, P. Bioorg. Med. Chem. Lett. 2011, 21, 510. https://doi.org/10.1016/j.bmcl.2010.10.091
  17. Peng, F. Y.; Xin, C. W.; Li, J. F.; Ji, D.; Bao, X. R.; Lu, J. R. Chin. J. Org. Chem. 2013, 33, 383. https://doi.org/10.6023/cjoc201209039
  18. Saikia, B.; Saikia, P. P.; Goswami, A.; Barua, N. C.; Saxena, A. K.; Suri, N. Synthesis 2011, 19, 3173.
  19. Aher, N. G.; Pore, V. S.; Mishra, N. N.; Kumar, A.; Shukla, P. P.; Sharma, A.; Bhak, M. K. Bioorg. Med. Chem. Lett. 2009, 19, 484.
  20. Boddy, I. K.; Briggs, G. G.; Harrison, R. P.; Jones, T. H.; Omahony, M. J.; Marlow, I. D.; Roberts, B. G.; Willis, R. J.; Bardsley, R.; Reid, J. Pestic. Sci. 1996, 48, 189. https://doi.org/10.1002/(SICI)1096-9063(199610)48:2<189::AID-PS461>3.0.CO;2-#
  21. Yan, M.; Shi, D. Q.; Xiao, L. X. Chin. J. Org. Chem. 2008, 28, 1012.
  22. Kuhnert, N.; Patel, C.; Jami, F. Tetrahedron Lett. 2005, 46, 7575-7579. https://doi.org/10.1016/j.tetlet.2005.08.155
  23. Bonnamour, J.; Legros, J.; Crousse, B.; Bonnet-Delpon, D. Tetrahedron Lett. 2007, 48, 8360-8362. https://doi.org/10.1016/j.tetlet.2007.09.118

Cited by

  1. Efficient synthesis of novel β-sitosterol scaffolds containing 1,2,3-triazole via copper(I)-catalyzed click reaction under microwave irradiation vol.72, pp.10, 2014, https://doi.org/10.1515/znb-2017-0074
  2. Discovery and Development of Inflammatory Inhibitors from 2-Phenylchromonone (Flavone) Scaffolds vol.20, pp.None, 2014, https://doi.org/10.2174/1568026620666200924115611