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Opening of 1-acylisatin ring in reactions with primary and secondary amines (microreview)

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Chemistry of Heterocyclic Compounds Aims and scope

This microreview compiles the methods of opening of 1-acylisatin ring in reactions with primary and secondary amines published over the past 8 years.

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References

  1. (a) Musin, L. I.; Bogdanov, A. V.; Mironov, V. F. Chem. Heterocycl. Compd. 2015, 51, 421. [Khim. Geterotsikl. Soedin. 2015, 51, 421.] (b) Singh, G. S.; Desta, Z. Y. Chem. Rev. 2012, 112, 6104. (c) Bogdanov, A. V.; Mironov, V. F. Chem. Heterocycl. Compd. 2016, 52, 90. [Khim. Geterotsikl. Soedin. 2016, 52, 90.] (d) Bogdanov, A. V.; Musin, L. I.; Mironov, V. F. ARKIVOC 2015, (vi), 362. (e) Borad, M. A.; Bhoi, M. N.; Prajapati, N. P.; Patel, H. D. Synth. Commun. 2014, 44, 897.

  2. (a) Li, H.; Cheng, B.; Boonnak, N.; Padwa, A. Tetrahedron 2011, 67, 9829. (b) Nizalapur, Sh.; Kimyon, O.; Yee, E.; Ho, K.; Berry, Th.; Manefield, M.; Cranfield, Ch. G.; Willcox, M. D.; Black, D. St. C.; Kumar, N. Org. Biomol. Chem. 2017, 15, 2033. (c) Nizalapur, Sh.; Ho, K. K. K.; Kimyon, O.; Yee, E.; Berry, Th.; Manefield, M.; Cranfield, Ch. G.; Willcox, M. D.; Black, D. St. C.; Kumar, N. Org. Biomol. Chem. 2016, 14, 3623. (d) Suryanti, V.; Bhadbhade, M.; Bishop, R.; Black, D. St. C.; Kumar, N. CrystEngComm 2012, 14, 7345. (e) Le, Th.; Cheah, W. Ch.; Wood, K.; Black, D. St. C.; Willcox, M. D.; Kumar, N. Tetrahedron Lett. 2011, 52, 3645. (f) Suryanti, V.; Bhadbhade, M.; Bishop, R.; Black, D. St. C.; Kumar, N. Tetrahedron 2013, 69, 8446. (g) Al-Wabli, R. I.; Salman, A.; Shyni, V.; Ghabbour, H. A.; Joe, I. H.; Almutairi, M. S.; Maklad, Y. A.; Attia, M. I. J. Mol. Struct. 2018, 1155, 457. (h) El-Faham, A.; Farooq, M.; Khattab, Sh. N.; Abutaha, N.; Wadaan, M. A.; Ghabbour, H. A.; Fun, H.-K. Molecules 2015, 20, 14638.

  3. (a) Ghazzali, M.; El-Faham, A.; Abdel-Megeed, A.; Al-Farhan, Kh. J. Mol. Struct. 2012, 1013, 163. (b) El-Faham, A.; Al Marhoon, Z.; Abdel-Megeed, A.; Siddiqui, M. J. Chem. 2013, Article ID 901745. (c) Suryanti, V.; Bhadbhade, M.; Chawla, H. M.; Howe, E.; Thordarson, P.; Black, D. St. C.; Kumar, N. Spectrochim. Acta Part A 2014, 121, 662. (d) El-Faham, A.; Al Marhoon, Z.; Abdel-Megeed, A.; Khattab, Sh. N.; Bekhit, A. A.; Albericio, F. Bioorg. Med. Chem. Lett. 2015, 25, 70. (e) El-Faham, A.; Al Marhoon, Z.; Abdel-Megeed, A.; Albericio, F. Molecules 2013, 18, 14747. (f) Andreani, A.; Burnelli, S.; Granaiola, M.; Leoni, A.; Locatelli, A.; Morigi, R.; Rambaldi, M.; Varoli, L.; Cremonini, M. A.; Placucci, G.; Cervellati, R.; Greco, E. Eur. J. Med. Chem. 2010, 45, 1374. (g) Shulga, S. I.; Simurova, N. V.; Shulga, О. S.; Misa, N. I. Russ. J. Org. Chem. 2014, 50, 1175. [Zh. Org. Khim. 2014, 50, 1192.]

  4. (a) Hossain, M. M.; Islam, R. M.; Saha, S. K.; Islam, M. K. Tetrahedron Lett. 2010, 51, 1155. (b) El-Faham, A.; Khattab, Sh. N.; Ghabbour, H. A.; Fun, H.-K.; Siddiqui, M. R. H. Chem. Cent. J. 2014, 8, 27. (c) Cheah, W. Ch.; Wood, K.; Black, D. St. C.; Kumar, N. Tetrahedron 2011, 67, 7603.

  5. Suryanti, V.; Condie, G. C.; Bhadbhade, M.; Bishop, R.; Black, D. St. C.; Kumar, N. Aust. J. Chem. 2014, 67, 1270.

  6. Xia, P.-J.; Xiao, J.-A.; Sun, Y.-H.; Li, J.; Xiang, H.-Y.; Chen, X.-Q.; Yang, H. Eur. J. Org. Chem. 2016, 30, 5096.

    Article  CAS  Google Scholar 

  7. Cheah, W. Ch.; Black, D. St. C.; Goh, W. K.; Kumar, N. Tetrahedron Lett. 2008, 49, 2965.

    Article  CAS  Google Scholar 

  8. Banerjee, P.; Pandey, A. K. RSC Adv. 2014, 4, 33236.

    Article  CAS  Google Scholar 

  9. (a) Mukhina, O. A.; Kuznetsov, D. M.; Cowger, T. M.; Kutateladze, A. G. Angew. Chem., Int. Ed. 2015, 54, 11516. (b) Son, J.-H.; Zhu, J. S.; Phuan, P.-W.; Cil, O.; Teuthorn, A. P.; Ku, C. K.; Lee, S.; Verkman, A. S.; Kurth, M. J. J. Med. Chem. 2017, 60, 2401. (c) Boraei, A. T. A.; El Tamany, E. S. H.; Ali, I. A. I.; Gebriel, S. M. J. Heterocycl. Chem. 2017, 54, 2881.

  10. Ibrahim, M. F.; Al-Karewi, A. A. A.; Khattab, S. N.; Hamed, E. A.; El-Faham, A. Asian J. Chem. 2014, 26, 8029.

    Article  CAS  Google Scholar 

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry of the Kazan Scientific Center, Russian Academy of Sciences, 8 Akademika Arbuzova St., Kazan, 420088, Russia

    Andrei V. Bogdanov & Ilyuza F. Zaripova

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  1. Andrei V. Bogdanov
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  2. Ilyuza F. Zaripova
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Correspondence to Andrei V. Bogdanov.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2018, 54(7), 686–688

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Bogdanov, A.V., Zaripova, I.F. Opening of 1-acylisatin ring in reactions with primary and secondary amines (microreview). Chem Heterocycl Comp 54, 686–688 (2018). https://doi.org/10.1007/s10593-018-2331-x

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  • DOI: https://doi.org/10.1007/s10593-018-2331-x

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