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Applications of thiobenzophenone for the synthesis of 3-, 4-, 5-, and 6-membered sulfur heterocycles (microreview)

  • HETEROCYCLES IN FOCUS
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Chemistry of Heterocyclic Compounds Aims and scope

The review summarizes representative applications of thiobenzophenone for the synthesis of sulfur heterocycles with diverse ring size.

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References

  1. (a) Huisgen, R.; Langhals, E. Tetrahedron Lett. 1989, 30, 5369. (b) Huisgen, R.; Fišera, L.; Giera, H.; Sustmann, R. J. Am. Chem. Soc. 1995, 117, 967. (c) Huisgen, R.; Langhals, E.; Li, X. Helv. Chim. Acta 2001, 84, 981. (d) Rohr, U.; Schatz, J.; Sauer, J. Eur. J. Org. Chem. 1998, 2875. (e) Schatz, J.; Sauer, J. Tetrahedron Lett. 1994, 35, 4767.

  2. Gattermann, L. Ber. Dtsch. Chem. Ges. 1895, 28, 2877.

    Article  Google Scholar 

  3. Arjuan, P.; Ramamurthy, V.; Venkatesan, K. J. Org. Chem. 1984, 49, 1765.

    Article  Google Scholar 

  4. (a) Kayukova, L. A.; Praliyev, K. D.; Gut'yar, V. G.; Baitursynova, G. P. Russ. J. Org. Chem. 2015, 51, 148. [Zh. Org. Khim. 2015, 51, 162.] (b) Varma, R. S.; Kumar, D. Org. Lett. 1999, 1, 697.

  5. Mlostoń, G.; Heimgartner, H. Helv. Chim. Acta 1996, 79, 1785.

    Article  Google Scholar 

  6. Mlostoń, G.; Romański, J.; Swiątek, A.; Heimgartner, H. Helv. Chim. Acta 1999, 82, 946.

    Article  Google Scholar 

  7. (a) Mlostoń, G.; Prakash, G. K. S.; Olah, G. A.; Heimgartner, H. Helv. Chim. Acta 2002, 85, 1644. (b) Large-Radix, S.; Billard, T.; Langlois, B. R. J. J. Fluorine Chem. 2003, 124, 147.

  8. Mlostoń, G.; Urbaniak, K.; Szychowska, A.; Linden, A.; Heimgartner, H. Heterocycles 2015, 90, 529.

    Article  Google Scholar 

  9. Huisgen, R.; Kalvinsch, I.; Li X.; Mlostoń, G. Eur. J. Org. Chem. 2000, 16685.

  10. Huisgen, R.; Li, X.; Giera, H.; Langhals, E. Helv. Chim. Acta 2001, 84, 981.

    Article  CAS  Google Scholar 

  11. Leśniak, S.; Mlostoń, G.; Urbaniak, K.; Wasiak, P.; Linden, A.; Heimgartner, H. Tetrahedron 2006, 62, 7776.

    Article  Google Scholar 

  12. Nikolaev, V. A.; Ivanov, A. V.; Shakhmin, A. A.; Sieler, J.; Rodina L. L. Tetrahedron Lett. 2012, 53, 3095.

    Article  CAS  Google Scholar 

  13. Dunstan, J. B. F.; Elsey, G. M.; Russell, R.A.; Savage, G. P.; Simpson, G. W.; Tiekink, E. R. T. Aust. J. Chem. 1998, 51, 499.

    Article  CAS  Google Scholar 

  14. Hewitt, R. J.; Ong, M. J. H.; Lim, Y. W.; Burkett, B. A. Eur. J. Org. Chem. 2015, 30, 6687.

    Article  Google Scholar 

  15. Breu, J.; Höcht, P.; Rohr, U.; Schatz, J.; Sauer, J. Eur. J. Org. Chem. 1998, 2861.

  16. Gotthardt, H.; Nieberl, S. Liebigs Ann. Chem. 1980, 867. (b) Mlostoń, G.; Grzelak, P.; Mikina, M.; Linden, A.; Heimgartner, H. Beilstein J. Org. Chem. 2015, 11, 576.

  17. Mlostoń, G.; Heimgartner, H. Helv. Chim. Acta 1995, 78, 1298.

    Article  Google Scholar 

  18. Huisgen, R.; Rapp, J. Heterocycles 1997, 45, 507.

    Article  CAS  Google Scholar 

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Authors and Affiliations

  1. Department of Organic and Applied Chemistry, University of Łódź, 12 Tamka, Łódź, 91-403, Poland

    Paulina Grzelak & Grzegorz Mlostoń

Authors
  1. Paulina Grzelak
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  2. Grzegorz Mlostoń
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Correspondence to Paulina Grzelak.

Additional information

Published in Khimiya Geterotsiklicheskikh Soedinenii, 2016, 52(5), 282–284

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Grzelak, P., Mlostoń, G. Applications of thiobenzophenone for the synthesis of 3-, 4-, 5-, and 6-membered sulfur heterocycles (microreview). Chem Heterocycl Comp 52, 282–284 (2016). https://doi.org/10.1007/s10593-016-1878-7

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  • DOI: https://doi.org/10.1007/s10593-016-1878-7

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