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Chemistry of Heterocyclic Compounds

, Volume 54, Issue 11, pp 1020–1022 | Cite as

Open image in new window Recent applications of isothiocyanates in thiophene synthesis (microreview)

  • Seyed Sajad Sajadikhah
  • Elham Jazinizadeh
Article
  • 22 Downloads

This microreview focuses on the recently published literature in 2013–2018 for the synthesis of thiophene derivatives based on isothiocyanates as key reactant.

Notes

Financial support from the Research Council of the Payame Noor University is gratefully acknowledged.

References

  1. 1.
    (a) Ruppel, J. V.; Snyder, N. L.; Thompson, A. D.; Farnsworth, T. W. Heterocyclic Chemistry in Drug Discovery; Li, J. J., Ed.; Wiley: Hoboken, 2013, p. 119. (b) Kostyuchenko, A. S.; Drozdova, E. A.; Fisyuk, A. S. Chem. Heterocycl. Compd. 2017, 53, 92. [Khim. Geterotsikl. Soedin. 2017, 53, 92.] (c) Eletheriadis, N.; Poelman, H.; Leus, N. G. J.; Honrath, B.; Neochoritis, C. G.; Dolga, A.; Domling, A.; Dekker, F. J. Eur. J. Med. Chem. 2016, 122, 786.Google Scholar
  2. 2.
    Grotkopp, O.; Müller, T. J. J. Chem. Heterocycl. Compd. 2017, 53, 66. [Khim. Geterotsikl. Soedin. 2017, 53, 66.]Google Scholar
  3. 3.
    (a) Nayak, K. R.; Cavendish, J. J. Vasc. Health Risk Manage. 2007, 3, 289. (b) Topol, E. J.; Schork, N. J. Nat. Med. 2011, 17, 40. (c) Chao, E. C. Drugs Future 2011, 36, 351.Google Scholar
  4. 4.
    Ali, K. A.; Abdalghfar, H. S.; Mahmoud, K.; Ragab, E. A. J. Heterocycl. Chem. 2013, 50, 1157.Google Scholar
  5. 5.
    Sable, P. N.; Ganguly, S.; Chaudhari, P. D. Chin. Chem. Lett. 2014, 25, 1099.CrossRefGoogle Scholar
  6. 6.
    Mabkhot, Y. N.; Alatibi, F.; El-Sayed, N. N. E.; Al-Showiman, S.; Kheder, N. A.; Wadood, A.; Rauf, A.; Bawazeer, S.; Hadda, T. B. Molecules 2016, 21, 222.CrossRefGoogle Scholar
  7. 7.
    Kim, J. K.; Lim, H. J.; Jeong, K. C.; Park, S. J. Beilstein J. Org. Chem. 2018, 14, 243.Google Scholar
  8. 8.
    Alizadeh, A.; Hosseiabadi, M.; Bayat, F. Phosphorus, Sulfur Silicon Relat. Elem. 2015, 190, 1056.Google Scholar
  9. 9.
    Nasr, T.; Bondock, S.; Eid, S. Eur. J. Med. Chem. 2014, 84, 491.CrossRefGoogle Scholar
  10. 10.
    Gouda, M. A. J. Heterocycl. Chem. 2017, 54, 268.CrossRefGoogle Scholar
  11. 11.
    Shvydenko, T.; Nazarenko, K.; Shvydenko, K.; Filimonchuk, S.; Vlasenko, Y.; Tolmachev, A.; Kostyuk, A. Tetrahedron Lett. 2016, 57, 1909.CrossRefGoogle Scholar
  12. 12.
    Acharya, A.; Kumar, S. V.; Saraiah, B.; Ila, H. J. Org. Chem. 2015, 80, 2884.CrossRefGoogle Scholar
  13. 13.
    Kim, K. H.; Lim, J. W.; Kim, S. Y.; Kim, J. N. Tetrahedron Lett. 2015, 56, 5799.CrossRefGoogle Scholar
  14. 14.
    (a) Nedolya, N. A.; Tarasova, O. A.; Albanov, A. I.; Trofimov, B. A. J. Org. Chem. 2017, 82, 7519. (b) Nedolya, N. A.; Tarasova, O. A.; Albanov, A. I.; Trofimov, B. A. Russ. J. Org. Chem. 2017, 53, 1272. [Zh. Org. Khim. 2017, 53, 1272.]Google Scholar

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© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of ChemistryPayame Noor UniversityTehranIran

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