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Chemistry of Heterocyclic Compounds

, Volume 54, Issue 10, pp 923–925 | Cite as

Open image in new window Methods for the synthesis of indole-3-carboxylic acid esters (microreview)

  • Valeriya A. Litvinova
  • Alexander S. Tikhomirov
Article
  • 51 Downloads

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In this microreview, recent advances in the development of methods for indole cyclization, leading to indole-3-carboxylic acid derivatives, are highlighted. Selected works published since 2013 are covered.

Notes

The material was prepared with the partial support of the Grants Council of the President of the Russian Federation for state support of young Russian scientists (grant МК-2474.2018.3)

References

  1. 1.
    Chadha, N.; Silakari, O. Eur. J. Med. Chem. 2017, 134, 159.Google Scholar
  2. 2.
    (a) Shchekotikhin, A. E.; Glazunova, V. A.; Dezhenkova, L. G.; Luzikov, Y. N.; Buyanov, V. V.; Treshalina, H. M.; Lesnaya, N. A.; Romanenko, V. I.; Kaluzhny, D. N.; Balzarini, J.; Agama, K.; Pommier, Y.; Shtil, A. A.; Preobrazhenskaya, M. N. Eur. J. Med. Chem. 2014 , 86, 797. (b) Tikhomirov, A. S.; Litvinova, V. A.; Luzikov, Y. N.; Korolev, A. M.; Sinkevich, Y. B.; Shchekotikhin, A. E. Chem. Heterocycl. Compd. 2017, 53, 1072. [Khim. Geterotsikl. Soedin. 2017, 53, 1072.]Google Scholar
  3. 3.
    Liu, X.-G.; Li, Z.-H.; Xie, J.-W.; Liu, Р.; Zhang, J.; Dai, В. Tetrahedron 2016, 72, 653.Google Scholar
  4. 4.
    Shen, D.; Han, J.; Chen, J.; Deng, H.; Shao, М.; Zhang, Н.; Cao, W. Org. Lett. 2015, 17, 3283.Google Scholar
  5. 5.
    Li, H.; Zhao, Y.; Ma, L.; Ma, M.; Jiang, J.; Wan, X. Chem. Commun. 2017, 53, 5993.Google Scholar
  6. 6.
    (a) Lv, H.; Shi, J.; Wu, В.; Guo, Y.; Huang, J.; Yi, W. Org. Biomol. Chem. 2017, 15, 8054. (b) Li, Y.; Li, J.; Wu, Х.; Zhou, Y.; Liu, H. J. Org. Chem 2017, 82, 8984. (c) Mishra, N. K.; Choi, М.; Jo, Н.; Oh, Y.; Sharma, S.; Han, S. H.; Jeong, T.; Han, S.; Lee, S.-Y.; Kim, I. S. Chem. Commun. 2015, 51, 17229. (d) Li, Y.; Qi, Z.; Wang, Н.; Yang, Х.; Li, X. Angew. Chem., Int. Ed. 2016, 55, 11877. (e) Jiang, H.; Gao, Sh.; Xu, J.; Wu, Х.; Lin, А.; Yao, Н. Adv. Synth. Catal. 2016, 358, 188. (f) Shi, P.; Wang, L.; Guo, S.; Chen, K.; Wang, J.; Zhu, J. Org. Lett. 2017, 19, 4359. (g) Patel, P.; Borah, G. Eur. J. Org. Chem. 2017, 2272.Google Scholar
  7. 7.
    Nguyen, H. H.; Kurth, M. J. Org. Lett. 2013, 15, 362.Google Scholar
  8. 8.
    Lian, X.-L.; Ren, Zh.-H.; Wang, Y.-Y.; Guan, Zh.-H. Org. Lett. 2014, 16, 3360.Google Scholar
  9. 9.
    (a) Zoller, J.; Fabry, D. C.; Ronge, M. A.; Rueping, M. Angew. Chem., Int. Ed. 2014, 53, 13264. (b) Wu, Ch.-J.; Meng, Q.; Lei, T.; Zhong, J.-J.; Liu, W.-Q.; Zhao, L.-M.; Li, Zh.-J.; Chen, B.; Tung, Ch.-H.; Wu, L.-Zh. ACS Catal. 2016, 6, 4635. (c) Liu, W.-Q.; Lei, Т.; Song, Z.-Q.; Yang, X.-L.; Wu, Ch.-J.; Jiang, X.; Chen, B.; Tung, Сh.-H.; Wu, L.-Zh. Org. Lett. 2017, 19, 3251.Google Scholar
  10. 10.
    Festa, A. Chem. Heterocycl. Compd. 2018, 54, 22. [Khim. Geterotsikl. Soedin. 2018, 54, 22.]Google Scholar
  11. 11.
    Tang, S.; Gao, X.; Lei, A. Chem. Commun. 2017, 53, 3354.Google Scholar
  12. 12.
    Gharpure, S. J.; Anuradha, D. Org. Lett. 2017, 19, 6136.Google Scholar
  13. 13.
    Bodunov, V. A.; Galenko, Е. Е.; Galenko, A. V.; Novikov, M. S.; Khlebnikov, A. F. Synthesis 2018, 2784.Google Scholar
  14. 14.
    Jiang, M.; Xiang, H.; Zhu, F.; Xu, X.; Deng, L.; Yang, C. Org. Biomol. Chem. 2015, 13, 10122.Google Scholar
  15. 15.
    Formenti, D.; Ferretti, F.; Ragaini, F. ChemCatChem 2018, 10, 148.Google Scholar
  16. 16.
    Baumann, M.; Baxendale, I. R.; Deplante, F. Beilstein J. Org. Chem. 2017, 13, 2549.Google Scholar

Copyright information

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

Authors and Affiliations

  • Valeriya A. Litvinova
    • 1
    • 2
  • Alexander S. Tikhomirov
    • 1
    • 2
  1. 1.Gause Institute of New AntibioticsMoscowRussia
  2. 2.D. Mendeleev University of Chemical Technology of RussiaMoscowRussia

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