Journal of the Korean Chemical Society (대한화학회지)

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Novel Synthesis of Thioflavones and Their Pyridyl Analogs from 2-Mercaptobenzoic(nicotinic) Acid

  • Lee, Jae In (Department of Chemistry, College of Science and Technology, Duksung Women's University)
  • Published : 2021.04.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Razdan, R. K.; Bruni, R. J.; Mehta, A. C.; Weinhardt, K. K.; Papanastassiou, Z. B. J. Med. Chem. 1978, 21, 643. https://doi.org/10.1021/jm00205a010
  2. Zhang, D.; Ji, X.; Gao, R.; Wang, H.; Meng, S.; Zhong, Z.; Li, Y.; Jiang, J.; Li, Z. Acta Pharm. Sin. B 2012, 2, 575. https://doi.org/10.1016/j.apsb.2012.10.005
  3. Jang, M.; Kim, G.-H. J. Food Saf. 2017, 37, e12337. https://doi.org/10.1111/jfs.12337
  4. (a) Wang, H.-K.; Bastow, K. F.; Cosentino, L. M.; Lee, K.-H. J. Med. Chem. 1996, 39, 1975. https://doi.org/10.1021/jm960008c
  5. (b) Kataoka, T.; Watanabe, S.; Mori, E.; Kadomoto, R.; Tanimura, S.;Kohno, M. Bioorg. Med. Chem. 2004, 12, 2397. https://doi.org/10.1016/j.bmc.2004.02.002
  6. Jang, E. J.; Seok, Y. M.; Lee, J. I.; Cho, H. M.; Sohn, U. D.; Kim, I. K. Naunyn-Schmiedeberg's Arch. Pharmacol. 2013, 386, 339. https://doi.org/10.1007/s00210-012-0818-z
  7. (a) Sosnovskikh, V. Y. Russ. Chem. Rev. 2018, 87, 49. https://doi.org/10.1070/RCR4756
  8. (b) Dong, J.; Zhang, Q.; Meng, Q.; Wang,Z.; Li, S.; Cui, J. Mini-Reviews Med. Chem. 2018, 18,1714. https://doi.org/10.2174/1389557518666180515145633
  9. Kobayashi, K.; Kobayashi, A.; Ezaki, K. Heterocycles 2012, 85, 1997. https://doi.org/10.3987/COM-12-12508
  10. Venkateswarlu, S.; Murty, G. N.; Satyanarayana, M.; Siddaiah, V. Synth. Commun. 2020, 50, 2347. https://doi.org/10.1080/00397911.2020.1775852
  11. Sangeetha, S.; Sekar, G. Org. Lett. 2019, 21, 75. https://doi.org/10.1021/acs.orglett.8b03508
  12. Kim, H. Y.; Song, E.; Oh, K. Org. Lett. 2017, 19, 312. https://doi.org/10.1021/acs.orglett.6b03348
  13. Wang, D.; Sun, P.; Jia, P.; Peng, J.; Yue, Y.; Chen, C. Synthesis 2017, 49, 4309. https://doi.org/10.1055/s-0036-1588466
  14. Yang, X.; Li, S.; Liu, H.; Jiang, Y.; Fu, H. RSC Adv. 2012, 2, 6549. https://doi.org/10.1039/c2ra20897k
  15. (a) Fuchs, F. C.; Eller, G. A.; Holzer, W. Molecules 2009, 14, 3814. https://doi.org/10.3390/molecules14093814
  16. (b) Lee, J. I. Bull. Kor. Chem. Soc. 2012, 33, 1375. https://doi.org/10.5012/bkcs.2012.33.4.1375
  17. Shen, C.; Spannenberg, A.; Wu, X.-F. Angew. Chem. Int. Ed. 2016, 55, 5067. https://doi.org/10.1002/anie.201600953
  18. Zhang, F.-L.; Chen, Z.-B.; Liu, K.; Yuan, Q.; Jiang, Q.; Zhu, Y.-M. Synlett 2018, 29, 621. https://doi.org/10.1055/s-0036-1591893
  19. (a) Willy, B.; Muller, T. J. J. Synlett 2009, 2009, 1255. https://doi.org/10.1055/s-0029-1216735
  20. (b) Willy, B.; Frank, W.; Muller, T. J. J. Org. Biomol. Chem. 2010, 8, 90. https://doi.org/10.1039/b917627f
  21. Lee, J. I. J. Kor. Chem. Soc. 2020, 64, 239. https://doi.org/10.5012/JKCS.2020.64.4.239
  22. (a) Lee, J. I. Bull. Kor. Chem. Soc. 2009, 30, 710. https://doi.org/10.5012/bkcs.2009.30.3.710
  23. (b) Lee, J. I.; Kim, M. J. Bull. Kor. Chem. Soc. 2011, 32, 1383. https://doi.org/10.5012/bkcs.2011.32.4.1383
  24. Shimizu, M.; Shimazaki, T.; Kon, Y.; Konakahara, T. Heterocycles 2010, 81, 413. https://doi.org/10.3987/COM-09-11859