Advertisement

Chemistry of Heterocyclic Compounds

, Volume 55, Issue 2, pp 126–128 | Cite as

Open image in new window Recent application of elemental sulfur in the synthesis of S-heterocycles (microreview)

  • Tímea Szabó
  • Mátyás MilenEmail author
Article
  • 81 Downloads

Sulfur-containing heterocycles represent an important class of organic compounds. Elemental sulfur plays a significant role in the synthesis of sulfur heterocycles. This microreview discusses some interesting examples published in 1999, 2014, and in the period from 2017 to 2019.

References

  1. 1.
    Pluth, M. D.; Bailey, T. S.; Hammers, M. D.; Hartle, M. D.; Henthorn, H. A.; Steiger, A. K. Synlett 2015, 2633.Google Scholar
  2. 2.
    Feng, M.; Tang, B.; Liang, S. H.; Jiang, X. Curr. Top. Med. Chem. 2016, 16, 1200.CrossRefGoogle Scholar
  3. 3.
    Roncali, J.; Blanchard, P.; Frère, P. J. Mater. Chem. 2005, 15, 1589.CrossRefGoogle Scholar
  4. 4.
    Je, S. H.; Buyukcakir, O.; Kim, D.; Coskun, A. Chem 2016, 1, 482.Google Scholar
  5. 5.
    Boyd, D. A. Angew. Chem., Int. Ed. 2016, 55, 15486.Google Scholar
  6. 6.
    Lim, J.; Pyun, J.; Char, K. Angew. Chem., Int. Ed. 2015, 54, 3249.CrossRefGoogle Scholar
  7. 7.
    Nguyen, T. B. Adv. Synth. Catal. 2017, 359, 1066.CrossRefGoogle Scholar
  8. 8.
    Liu, H.; Jiang, X. Chem.–Asian J. 2013, 8, 2546.CrossRefGoogle Scholar
  9. 9.
    Sakai, N.; Horikawa, S.; Ogiwara, Y. Synthesis 2018, 565.Google Scholar
  10. 10.
    Hu, Y.; Yin, Z.; Werner, T.; Spannenberg, A.; Wu, X.-F. Eur. J. Org. Chem. 2018, 1274.Google Scholar
  11. 11.
    Ying, J.; Wang, H.; Qi, X.; Peng, J.-B.; Wu, X.-F. Eur. J. Org. Chem. 2018, 688.Google Scholar
  12. 12.
    Sabnis, R. W.; Ragnekar, D. W.; Sonawane, N. D. J. Heterocycl. Chem. 1999, 36, 333.CrossRefGoogle Scholar
  13. 13.
    Joule, J. A. In Topics in Heterocyclic Chemistry; Joule, J. A., Ed.; Springer-Verlag: Berlin, Heidelberg, 2014, p. 26.Google Scholar
  14. 14.
    Ni, P.; Li, B.; Huang, H.; Xiao, F.; Deng, G.-J. Green Chem. 2018, 23, 5553.Google Scholar
  15. 15.
    Nguyen, B. T.; Retailleau, P. Org. Lett. 2017, 19, 4858.CrossRefGoogle Scholar
  16. 16.
    Wang, Z.; Qu, Z.; Xiao, F.; Huang, H.; Deng, G.-J. Adv. Synth. Catal. 2018, 360, 796.CrossRefGoogle Scholar
  17. 17.
    Adib, M.; Rajai-Daryasarei, S.; Pashazadeh, R.; Jahani, M.; Amanlou, M. Synlett 2018, 1583.Google Scholar
  18. 18.
    Liu, Z.; Gao, R.; Lou, J.; He, Y.; Yu, Z. Adv. Synth. Catal. 2018, 360, 3097.CrossRefGoogle Scholar
  19. 19.
    Nguyen, L. A.; Ngo, Q. A.; Retailleau, P.; Nguyen, T. B. Green Chem. 2017, 19, 4289.CrossRefGoogle Scholar
  20. 20.
    Xing, Q.; Ma, Y.; Xie, H.; Xiao, F.; Zhang, F.; Deng, G.-J. J. Org. Chem. 2019, 84, 1238.CrossRefGoogle Scholar
  21. 21.
    Yang, Z.; Hu, R.; Li, X.; Wang, X.; Gu, R.; Han, S. Tetrahedron Lett. 2017, 58, 2366.CrossRefGoogle Scholar
  22. 22.
    Wang, X.; Li, X.; Hu, R.; Yang, Z.; Gu, R.; Ding, S.; Li, P.; Han, S. Synlett 2018, 219.Google Scholar
  23. 23.
    Che, X.; Jiang, J.; Xiao, F.; Huang, H.; Deng, G.-J. Org. Lett. 2017, 19, 4576.CrossRefGoogle Scholar
  24. 24.
    Wang, Z.; Xie, H.; Xiao, F.; Guo, Y.; Huang, H.; Deng, G.-J. Eur. J. Org. Chem. 2017, 1604.Google Scholar
  25. 25.
    Zhou, Z.; Liu, M.; Sun, S.; Yao, E.; Liu, S.; Wu, Z.; Yu, J.-T.; Jiang, Y.; Cheng, J. Tetrahedron Lett. 2017, 58, 2571.CrossRefGoogle Scholar
  26. 26.
    Pournara, D.; Heropoulos, A. G.; Koufaki, M. Tetrahedron Lett. 2017, 58, 2378.CrossRefGoogle Scholar
  27. 27.
    Nguyen, T. B.; Retailleau, P. Org. Lett. 2017, 19, 3879.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Egis Pharmaceuticals PLCBudapestHungary

Personalised recommendations