Journal of the Korean Chemical Society (대한화학회지)

Korean Chemical Society (대한화학회)
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One-pot Synthesis of (Z)-Thioaurones from N-Methoxy-N-methyl 2-mercaptobenzamide and Arylethynyllithiums

  • Lee, Jae In (Department of Chemistry, College of Natural Science, Duksung Women's University)
  • Received : 2019.07.03
  • Accepted : 2019.07.25
  • Published : 2019.10.20
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References

  1. (a) Erdelyi, M.; Varedian, M.; Skold, C.; Niklasson, I. B.; Nurbo, J.; Persson, A.; Bergquist, J.; Gogoll, A. Org. Biomol. Chem. 2008, 6, 4356. https://doi.org/10.1039/b812001c
  2. (b) Plotner, J.; Dreuw, A. J. Phys. Chem. A 2009, 113, 11882. https://doi.org/10.1021/jp903156j
  3. (c) Maerz, B.; Wiedbrauk, S.; Oesterling, S.; Samoylova, E.; Nenov, A.; Mayer, P.; Vivie-Riedle, R.; Zinth, W.; Dube, H. Chem. Eur. J. 2014, 20, 13984. https://doi.org/10.1002/chem.201403661
  4. (d) Wiedbrauk, S.; Dube, H. Tetrahedron Lett. 2015, 56, 4266. https://doi.org/10.1016/j.tetlet.2015.05.022
  5. (e) Zweig, J. E.; Newhouse, T. R. J. Am. Chem. Soc. 2017, 139, 10956. https://doi.org/10.1021/jacs.7b04448
  6. (a) Konieczny, M. T.; Konieczny, W.; Okabe, S.; Tsujimoto, H.; Suda, Y.; Wierzba, K. Chem. Pharm. Bull. 2006, 54, 350. https://doi.org/10.1248/cpb.54.350
  7. (b) Mouineer, A. A.; Zaher, A. F.; El-malah, A. A.; Sobh, E. A. Miditerr. J. Chem. 2017, 6, 165. https://doi.org/10.13171/mjc65/01709262240-zaher
  8. Hallgas, B.; Patonay, T.; Kiss-Szikszai, A.; Dobos, Z.; Hollosy, F.; Eros, D.; Orfi, L.; Keri, G.; Idei, M. J. Chromato. B 2004, 801, 229. https://doi.org/10.1016/j.jchromb.2003.11.021
  9. Konieczny, M. T.; Konieczny, W. Heterocycles 2005, 65, 451. https://doi.org/10.3987/REV-04-590
  10. (a) Steinle, W.; Ruck-Braun, K. Org. Lett. 2003, 5, 141. https://doi.org/10.1021/ol027102+
  11. (b) Herre, S.; Steinle, W.; Ruck-Braun, K. Synthesis 2005, 2005, 3297.
  12. Benferraha, N.; Hammadia, M.; Villeminc, D. J. Chem. Pharm. Res. 2016, 8, 75.
  13. (a) Boughaleb, A.; Houari, G. A.; Bennani, B.; Daoudi, M.; Garrigues, B.; Kerbal, A.; Yazidi, M. E. J. Soc. Chim. Tunisie 2010, 12, 109.
  14. (b) Bakhouch, M.; Houari, G. A.; Daoudi, M.; Kerbal, A.; Yazidi, M. E. Mediterr. J. Chem. 2015, 4, 9. https://doi.org/10.13171/mjc.4.1.2015.16.02.23/elyazidi
  15. Cabiddu, M. G.; Cabiddu, S.; Cadoni, E.; Montis, S. D.; Fattuoni, C.; Melis, S.; Usai, M. Synthesis 2002, 2002, 875. https://doi.org/10.1055/s-2002-28523
  16. (a) Pradhan, T. K.; De, A.; Mortier, J. Tetrahedron 2005, 61, 9007. https://doi.org/10.1016/j.tet.2005.07.050
  17. (b) Kamila, S.; Mukherjee, C.; Pradhan, T. K.; De, A. Arkivoc 2006, 45.
  18. Zheng, G.; Ma, X.; Liu, B.; Dong, Y.; Wang, M. Adv. Synth. Catal. 2014, 356, 743. https://doi.org/10.1002/adsc.201300815
  19. Nguyen, T. B.; Retailleau, P. Org. Lett. 2018, 20, 186. https://doi.org/10.1021/acs.orglett.7b03547
  20. Lee, J. I. Bull. Korean Chem. Soc. 2019, 40, 70. https://doi.org/10.1002/bkcs.11637
  21. (a) Lee, J. I. Bull. Korean Chem. Soc. 2008, 29, 1263. https://doi.org/10.5012/bkcs.2008.29.6.1263
  22. (b) Lee, J. I. Bull. Korean Chem. Soc. 2009, 30, 710. https://doi.org/10.5012/bkcs.2009.30.3.710
  23. (c) Choi, E. J.; Lee, J. I.; Kim, G.-H. Int. J. Mol. Med. 2012, 29, 252. https://doi.org/10.3892/ijmm.2011.834
  24. (d) 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
  25. (e) Lee, J. I.; Lee, J.-H. Food Sci. Biotechnol. 2014, 23, 957. https://doi.org/10.1007/s10068-014-0129-x
  26. Legrand, S.; Nordlander, G.; Nordenhem, H.; Borg-Karlson, A.-K.; Unelius, C. R. Z. Naturforsch. 2004, 59b, 829. https://doi.org/10.1515/znb-2004-0714