Advertisement

Russian Journal of General Chemistry

, Volume 89, Issue 6, pp 1307–1309 | Cite as

Synthesis of Functional Derivatives of Benzofuran-5,6-dicarboxylic Acids

  • Zh. V. ChirkovaEmail author
  • S. I. Filimonov
  • I. G. Abramov
Article

Abstract

Synthetic routes to novel substituted benzofuran-5,6-dicarboxylic acids and furo[2,3-f]isoindole-5,7-diones via acid hydrolysis of the corresponding benzofuran-5,6-dicarbonitriles were developed.

Keywords

benzofuran-5,6-dicarbonitriles benzofuran-5,6-dicarboxylic acids furo[2,3-f]isoindole-5,7-diones 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Khanam, S.H., Eur. J. Med. Chem., 2015, vol. 97, p. 483. doi  https://doi.org/10.1016/j.ejmech.2014.11.039 CrossRefGoogle Scholar
  2. 2.
    Rajeshwari, K.Ch., Hiremathad, A., Singh, M., Santos, M.A., and Keri, R.S., Pharm. Rep, 2017, vol. 69, p. 281. doi  https://doi.org/10.1016/j.pharep.2016.11.007 CrossRefGoogle Scholar
  3. 3.
    Zhang, Y. and Herndon, J.W., J. Org. Chem., 2002, vol. 67, p. 4177. doi  https://doi.org/10.1021/jo011136y CrossRefGoogle Scholar
  4. 4.
    Zhang, Y. and Herndon, J.W., Tetrahedron Lett., 2001, vol. 42, p. 777. doi  https://doi.org/10.1016/S0040-4039(00)02123-7 CrossRefGoogle Scholar
  5. 5.
    Kalindjian, S.B., Buck, I.M., Davies, J.M.R., Dunstone, D.J., Hudson, M.L., Low, C.M.R., McDonald, I.M., Pether, M.J., Steel, K.I.M., Tozer, M.J., and Vinter, J.G., J. Med. Chem., 1996, vol. 39, p. 1806. doi  https://doi.org/10.1021/jm9508907 CrossRefGoogle Scholar
  6. 6.
    Min, B.K., Lim, J.W., Roh, H.J., and Kim, J.N., Bull. Korean Chem. Soc., 2016, vol. 37, p. 1724. doi  https://doi.org/10.1002/bkcs.10919 CrossRefGoogle Scholar
  7. 7.
    Harin, M.A., Pautet, F., Fillion, H., Domard, M., and Fenet, B., Tetrahedron, 1995, vol. 51, p. 9595. doi  https://doi.org/10.1016/0040-4020(95)00534-F CrossRefGoogle Scholar
  8. 8.
    Filimonov, S.I., Chirkova, Zh.V., Abramov, I.G., Shashkov, A.S., Firgang, S.I., and Stashina, G.A., Mendeleev Commun., 2009, vol. 19, p. 332. doi  https://doi.org/10.1016/j.mencom.2009.11.013 CrossRefGoogle Scholar
  9. 9.
    Eastmond, G.C., Paprotny, J., Pethrick, R.A., and Santamaria-Mendi, F., Macromolecules, 2006, vol. 39, p. 7534. doi  https://doi.org/10.1021/ma0524732 CrossRefGoogle Scholar
  10. 10.
    Ma, X., Ghanem, B., Salines, O., Litwiller, E., and Pinnau, I., ACS Macro Lett., 2015, vol. 4, p. 231. doi  https://doi.org/10.1021/acsmacrolett.5b00009 CrossRefGoogle Scholar
  11. 11.
    Tkachuk, V.A., Omelchenko, I.V., and Hordiyenko, O.V., Synlett, 2017, vol. 28, p. 851. doi  https://doi.org/10.1055/s-0036-1588933 CrossRefGoogle Scholar
  12. 12.
    Carvalho, C.F. and Sargent, M.V., J. Chem. Soc. Perkin Trans. 1, 1984, p. 1605. doi  https://doi.org/10.1039/P19840001605 Google Scholar
  13. 13.
    Chirkova, Zh.V., Kabanova, M.V., Luferenko, D.V., Filimonov, S.I., and Abramov, I.G., Russ. J. Org. Chem., 2015, vol. 51, p. 644. doi  https://doi.org/10.1134/S1070428015050103 CrossRefGoogle Scholar

Copyright information

© Pleiades Publishing, Ltd 2019

Authors and Affiliations

  • Zh. V. Chirkova
    • 1
    Email author
  • S. I. Filimonov
    • 1
  • I. G. Abramov
    • 1
  1. 1.Yaroslavl State Technical UniversityYaroslavlRussia

Personalised recommendations