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Usp. Khim., 2012, Volume 81, Issue 6, Pages 494–523 (Mi rcr24)  

This article is cited in 16 scientific papers (total in 16 papers)

Thiosemicarbazides in the synthesis of five- and six-membered heterocyclic compounds

G. A. Gazieva, A. N. Kravchenko

N.D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences

Abstract: Data on key chemical transformations of thiosemicarbazides resulting in heterocyclic compounds are generalized and described systematically. Methods for the synthesis of five- and six-membered heterocycles with two and three heteroatoms are considered. The bibliography includes 190 references.

Full text: http://www.uspkhim.ru/.../paper_rus.phtml?journal_id=rc&paper_id=4235

English version:
Russian Chemical Reviews, 2012, 81:6, 494–523

Bibliographic databases:

Received: 17.06.2011

Citation: G. A. Gazieva, A. N. Kravchenko, “Thiosemicarbazides in the synthesis of five- and six-membered heterocyclic compounds”, Usp. Khim., 81:6 (2012), 494–523; Russian Chem. Reviews, 81:6 (2012), 494–523

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    Citing articles on Google Scholar: Russian citations, English citations
    Related articles on Google Scholar: Russian articles, English articles

    This publication is cited in the following articles:
    1. Gazieva G.A., Poluboyarov P.A., Popov L.D., Kolotyrkina N.G., Kravchenko A.N., Makhova N.N., Synthesis, 44:21 (2012), 3366–3370  crossref  isi  elib  scopus
    2. G.A.. Gazieva, P.A.. Poluboyarov, Natal’ya.G.. Kolotyrkina, E.D.. Lubuzh, A.N.. Kravchenko, Mendeleev Communications, 24:1 (2014), 42  crossref  isi  elib  scopus
    3. G.A.. Gazieva, T.B.. Karpova, L.D.. Popov, Yu.V.. Nelyubina, A.N.. Kravchenko, J. Heterocyclic Chem, 2014, n/a  crossref  isi  scopus
    4. G.A.. Gazieva, A.N.. Izmest'ev, Yu.V.. Nelyubina, N.G.. Kolotyrkina, I.E.. Zanin, RSC Adv, 5:55 (2015), 43990  crossref  isi  elib  scopus
    5. Kudryavtseva T.N., Sysoev P.I., Popkov S.V., Nazarov G.V., Klimova L.G., Russ. Chem. Bull., 64:2 (2015), 445–450  crossref  isi  elib  scopus
    6. Belen'kii L.I. Evdokimenkova Yu.B., Advances in Heterocyclic Chemistry, Vol 116, Adv. Heterocycl. Chem., 116, ed. Scriven E. Ramsden C., Elsevier Academic Press Inc, 2015, 193–363  crossref  isi  scopus
    7. Fesenko A.A., Shutalev A.D., Tetrahedron, 72:20 (2016), 2560–2573  crossref  isi  scopus
    8. Gazieva G.A., Anikina L.V., Pukhov S.A., Karpova T.B., Nelyubina Yu.V., Kravchenko A.N., Mol. Divers., 20:4 (2016), 837–846  crossref  isi  scopus
    9. Bekircan O., Baltas N., Mentese E., Gultekin E., Rev. Roum. Chim., 61:10 (2016), 733–746  isi
    10. Pulatov E.Kh., Isobaev M.J., Mavlonov B.G., Russ. Chem. Bull., 65:10 (2016), 2475–2478  crossref  isi  scopus
    11. A. G. Mal'kina, V. V. Nosyreva, A. I. Albanov, A. V. Afonin, A. V. Vashchenko, S. V. Amosova, B. A. Trofimov, Synth. Commun., 47:2 (2017), 159–168  crossref  isi  scopus
    12. A. G. Mal'kina, V. V. Nosyreva, A. V. Afonin, A. I. Albanov, Q. A. Apartsin, E. G. Grigor'ev, B. A. Trofimov, Russ. J. Organ. Chem., 53:8 (2017), 1226–1232  crossref  isi  scopus
    13. A. D. Voloshina, V. E. Semenov, A. S. Strobykina, N. V. Kulik, E. S. Krylova, V. V. Zobov, V. S. Reznik, Russ. J. Bioorg. Chem., 43:2 (2017), 170–176  crossref  isi  scopus
    14. Ali B., Khan Kh.M., Salar U., Kanwal, Hussain S., Ashraf M., Riaz M., Wadood A., Taha M., Perveen Sh., Bioorganic Chem., 79 (2018), 363–371  crossref  isi  scopus
    15. Pyrih A., Berninger M., Gzella A., Lesyk R., Holzgrabe U., Synth. Commun., 48:14 (2018), 1883–1891  crossref  isi  scopus
    16. Krayushkin M.M., Yarovenko V.N., Zavarzin V I., Russ. Chem. Bull., 68:6 (2019), 1143–1163  crossref  isi
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