Chemistry of Heterocyclic Compounds

, Volume 54, Issue 6, pp 590–592 | Cite as

Open image in new window Synthesis of pyrano[3,4-c]pyrroles (microreview)

  • Mikhail Yu. IevlevEmail author
  • Oleg V. Ershov

This microview compiles approaches to the synthesis of derivatives of pyrano[3,4-c]pyrrole not condensed with other cyclic fragments covered in the literature starting from 2007.


The work was carried out within the framework of scholarship SP-127.2016.4 from the President of the Russian Federation for young scientists and graduate students.


  1. 1.
    DeVita, R. J.; Jiang, J.; Mills., S. G.; Young, J. R. US Patent 20080108689.Google Scholar
  2. 2.
    Millan, M. J.; Buccafusco, J. J.; Loiseau, F.; Watson, D. J.; Decamp, E.; Fone, K. C.; Thomasson-Perret, N.; Hill, M.; Mocaer, E.; Schneider, J. S. Int. J. Neuropsychopharmacol. 2010, 13, 1035.CrossRefPubMedGoogle Scholar
  3. 3.
    Hancock, A. A.; Buckner, S. A.; Brune, M. E.; Esbenshade, T. A.; Ireland, L. M; Katwala, S.; Milicic, I.; Meyer, M. D.; Kerwin, J. F., Jr.; Williams, M. J. Pharmacol. Exp. Ther. 2002, 300, 478.Google Scholar
  4. 4.
    Korotaev, V. Yu.; Kutyashev, I. B.; Barkov, A. Yu.; Sosnovskikh, V. Ya. Chem. Heterocycl. Compd. 2017, 53, 1192. [Khim. Geterotsikl. Soedin. 2017, 53, 1192.]Google Scholar
  5. 5.
    Zhang, J.; Zhang, Y.; Zhang, W.; Liu, B.; Zhang, J.; Liu, J.; Zhang, L. WO Patent 2013071697.Google Scholar
  6. 6.
    Kharaneko, O. I.; Bogza, S. L. Chem. Heterocycl. Compd. 2013, 48, 1734. [Khim. Geterotsikl. Soedin. 2012, 1849.]Google Scholar
  7. 7.
    Kharaneko, O. I.; Bogza, S. L. Russ. J. Org. Chem. 2016, 52, 1043. [Zh. Org. Khim. 2016, 52, 1049.]Google Scholar
  8. 8.
    Kharaneko, O. I. Russ. J. Org. Chem. 2016, 52, 1593. [Zh. Org. Khim. 2016, 52, 1600.]Google Scholar
  9. 9.
    Lowe, M. A.; Ostovar, M.; Ferrini, S.; Chen, C. C.; Lawrence, P. G.; Fontana, F.; Calabrese, A. A.; Aggarwal, V. K. Angew. Chem., Int. Ed. 2011, 50, 6370.Google Scholar
  10. 10.
    Zhang, S.; Ma, Y.; Lan, J.; Song, F.; You, J. Org. Biomol. Chem. 2015, 13, 5867.CrossRefPubMedGoogle Scholar
  11. 11.
    Fujii, M.; Yokoshima, S.; Fukuyama, T. Eur. J. Org. Chem. 2014, 22, 4823.CrossRefGoogle Scholar
  12. 12.
    Farwick, A.; Helmchen, G. Org. Lett. 2010 , 12, 1108.CrossRefPubMedGoogle Scholar
  13. 13.
    Takayama, H.; Jia, Z.-J.; Kremer, L.; Bauer, J. O.; Strohmann, C.; Ziegler, S.; Antonchick, A. P.; Waldmann, H. Angew. Chem., Int. Ed. 2013, 52, 12404.Google Scholar
  14. 14.
    Udry, G. A. O.; Repetto, E.; Varela, O. J. Org. Chem. 2014, 79, 4992.CrossRefGoogle Scholar
  15. 15.
    Udry, G. A. O.; Repetto, E.; Vega, D. R.; Varela, O. J. Org. Chem. 2016, 81, 4179.CrossRefGoogle Scholar
  16. 16.
    Sakaguchi, H.; Tokuyama, H.; Fukuyama, T. Org. Lett. 2007, 9, 1635.CrossRefPubMedGoogle Scholar
  17. 17.
    Sakaguchi, H.; Tokuyama, H.; Fukuyama, T. Org. Lett. 2008, 10, 1711.CrossRefPubMedGoogle Scholar
  18. 18.
    Tanaka, K.; Otake, Y.; Sagae, H.; Noguchi, K.; Hirano, M. Angew. Chem., Int. Ed. 2008, 47, 1312.Google Scholar
  19. 19.
    Ishida, M.; Tanaka, K. Org. Lett. 2013, 15, 2120.CrossRefPubMedGoogle Scholar
  20. 20.
    Kossler, D.; Cramer, N. J. Am. Chem. Soc. 2015, 137, 12478.CrossRefPubMedGoogle Scholar
  21. 21.
    Furstner, A.; Stimson, C. C. Angew. Chem., Int. Ed. 2007, 46, 8845.Google Scholar
  22. 22.
    Koo, J.; Park, H.-S.; Shin, S. Tetrahedron Lett. 2013, 54, 834.CrossRefGoogle Scholar
  23. 23.
    Ishii, M.; Mori, F.; Tanaka, K. Chem.–Eur. J. 2014, 20, 2169.Google Scholar
  24. 24.
    Yamazaki, S.; Sugiura, H.; Ohashi, S.; Ishizuka, K. Saimu, R.; Mikata, Y.; Ogawa, A. J. Org. Chem. 2016, 81, 10863.CrossRefPubMedGoogle Scholar
  25. 25.
    Gao, Q.; Hao, W.-J.; Liu, F.; Tu, S.-J.; Wang, S.-L.; Li, G.; Jiang, B. Chem. Commun. 2016, 52, 900.CrossRefGoogle Scholar
  26. 26.
    Ievlev, M. Yu.; Ershov, O. V.; Tafeenko, V. A. Org. Lett. 2016, 18, 1940.CrossRefPubMedGoogle Scholar
  27. 27.
    Ievlev, M. Yu.; Ershov, O. V.; Vasil'ev, A. N.; Tafeenko, V. A.; Surazhskaya, M. D.; Nasakin, O. E. Russ. J. Org. Chem. 2017, 53, 1030. [Zh. Org. Khim. 2017, 53, 1019.]Google Scholar

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

Authors and Affiliations

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

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