Advertisement

Chemistry of Heterocyclic Compounds

, Volume 52, Issue 5, pp 279–281 | Cite as

Synthesis of 3H-pyrroles (microreview)

  • Mikhail Yu. BelikovEmail author
  • Oleg V. Ershov
HETEROCYCLES IN FOCUS
In this microreview, the approaches to the construction of non-condensed 3H-pyrrole ring based mainly on reactions of isonitriles, nitriles, and oximes described in the literature over the past 10 years are presented.

Keywords

Ketone Acetylene Oxime Phosphite Corrosion Inhibitor 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

The work was supported by the President of Russia scholarship for young scientists and postgraduate students No. SP-2501.2016.4.

References

  1. 1.
    Shimkin, A. A.; Shirinian, V. Z.; Nikalin, D. M.; Krayushkin, M. M.; Pivina, T. S.; Troitsky, N. A.; Vorontsova, L. G.; Starikova, Z. A. Eur. J. Org. Chem. 2006, 2087.Google Scholar
  2. 2.
    Welch, K. D.; Smith, P. L.; Keller, A. P.; Myers, W. H.; Sabat, M.; Harman, W. D. Organometallics 2006, 25, 5067.CrossRefGoogle Scholar
  3. 3.
    Perrin, S.; Monnier, K.; Laude, B. J. Chem. Res. (S) 1997, 104.Google Scholar
  4. 4.
    Chiu, P.-K.; Sannes, M. P. Tetrahedron 1990, 46, 3439.CrossRefGoogle Scholar
  5. 5.
    Lui, K. H.; Lai, T. F.; Sammes, M. P. J. Chem. Res. (M) 1989, 1759.Google Scholar
  6. 6.
    Perrin, S.; Monnier, K.; Laude, B. Bull. Soc. Chim. Belg. 1996, 105, 777.Google Scholar
  7. 7.
    Schmitt, G.; Nasser, B.; An, N. D.; Laude, B.; Roche, M. Can. J. Chem. 1990, 68, 863.CrossRefGoogle Scholar
  8. 8.
    Trofimov, B. A.; Shevchenko, S. G.; Korostova, S. E.; Mikhaleva, A. I.; Sigalov, M. V.; Krivdin, L. B. Chem. Heterocycl. Compd. 1989, 25, 1314. [Khim. Geterotsikl. Soedin. 1989, 1566.]Google Scholar
  9. 9.
    Padmavathi, V.; Radha, L. T.; Mahesh, K.; Padmaja, A. Chem. Pharm. Bull. 2009, 57, 1200.CrossRefGoogle Scholar
  10. 10.
    Cirrincione, G.; Almerico, A. M.; Grimaudo, S.; Diana, P.; Mingoia, F.; Barraja, P.; Misuraca, F. Farmaco 1996, 51, 49.Google Scholar
  11. 11.
    Cirrincione, G.; Almerico, A. M.; Dattolo, G.; Aiello, E.; Grimaudo, S.; Diana, P.; Misuraca, F. Farmaco 1992, 47, 1555.Google Scholar
  12. 12.
    Shabalin, D. A.; Dvorko, M. Yu.; Schmidt, E. Yu.; Ushakov, I. A.; Protsuk, N. I.; Kobychev, V. B.; Soshnikov, D. Yu.; Trofimov, A. B.; Vitkovskaya, N. M.; Mikhaleva, A. I.; Trofimov, B. A. Tetrahedron 2015, 71, 3273.CrossRefGoogle Scholar
  13. 13.
    Shabalin, D. A.; Schmidt, E. Yu.; Dvorko, M. Yu.; Protsuk, N. I.; Ushakov, I. A.; Trofimov, B. A. Russ. J. Org. Chem. 2015, 51, 1346. [Zh. Org. Khim. 2015, 51, 1372.].Google Scholar
  14. 14.
    Shabalin, D. A.; Glotova, T. E.; Ushakov, I. A.; Dvorko, M. Yu.; Vashchenko, A. V.; Smirnov, V. I.; Schmidt, E. Yu.; Mikhaleva, A. I.; Trofimov, B. A. Mendeleev Commun. 2014, 24, 368.CrossRefGoogle Scholar
  15. 15.
    Ichikawa, J.; Sakoda, K.; Mihara, J.; Ito, N. J. Fluorine Chem. 2006, 127, 489.CrossRefGoogle Scholar
  16. 16.
    Sakoda, K.; Mihara, J.; Ichikawa, J. Chem. Commun. 2005, 4684.Google Scholar
  17. 17.
    Liao, J.-Y.; Shao, P.-L.; Zhao Y. J. Am. Chem. Soc. 2015, 137, 628.CrossRefGoogle Scholar
  18. 18.
    Yavari, I.; Ghanbari, E.; Hosseinpour, R. Helv. Chim. Acta. 2014, 97, 1004.CrossRefGoogle Scholar
  19. 19.
    Das, P.; Ray, S.; Mukhopadhyay, C. Org. Lett. 2013, 15, 5622.CrossRefGoogle Scholar
  20. 20.
    Verma, C. B.; Ebenso, E. E.; Bahadur, I.; Obot, I. B.; Quraishi, M. A. J. Mol. Liq. 2015, 212, 209.CrossRefGoogle Scholar
  21. 21.
    Belikov, M. Yu.; Ershov, O. V.; Eremkin, A. V.; Nasakin, O. E.; Tafeenko, V. A.; Nurieva, E. V. Tetrahedron Lett. 2011, 52, 6407.CrossRefGoogle Scholar
  22. 22.
    Belikov, M. Yu.; Ershov, O. V.; Lipovskaya, I. V.; Eremkin, A. V.; Nasakin, O. E. Russ. J. Org. Chem. 2011, 47, 1401. [Zh. Org. Khim. 2011, 47, 1426.]Google Scholar
  23. 23.
    Belikov, M. Yu.; Ershov, O. V.; Lipovskaya, I. V.; Fedoseev, S. V.; Nasakin, O. E. Russ. J. Org. Chem. 2013, 49, 864. [Zh. Org. Khim. 2013, 49, 880.]Google Scholar
  24. 24.
    Belikov, M. Yu.; Ershov, O. V.; Lipovskaya, I. V.; Fedoseev, S. V.; Lipin, K. V.; Nasakin O. E. Russ. J. Org. Chem. 2013, 49, 1195. [Zh. Org. Khim. 2013, 49, 1211.]Google Scholar
  25. 25.
    Ershov, O. V.; Belikov, M. Yu.; Nasakin, O. E. RU Patent 2475489 C1, 2013.Google Scholar
  26. 26.
    Belikov, M. Yu.; Ievlev, M. Yu.; Belikova, I. V.; Ershov, O. V.; Tafeenko, V. A.; Surazhskaya, M. D. Chem. Heterocycl. Compd. 2015, 51, 518. [Khim. Geterotsikl. Soedin. 2015, 51, 518.]Google Scholar

Copyright information

© Springer Science+Business Media New York 2016

Authors and Affiliations

  1. 1.Chuvash State University named after I. N. UlyanovCheboksaryRussia

Personalised recommendations