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Russian Chemical Reviews, 2020, Volume 89, Issue 7, Pages 750–786
DOI: https://doi.org/10.1070/RCR4913 (Mi rcr4301) 		 
This article is cited in 16 scientific papers (total in 16 papers)

Aromatic and heteroaromatic azacrown compounds: advantages and disadvantages of rigid macrocyclic ligands

A. D. Zubenko, O. A. Fedorova

A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, Moscow
English full-text Citations (16) Russian version article
DOI: https://doi.org/10.1070/RCR4913
Abstract: Current approaches to the synthesis of aromatic and heteroaromatic azamacrocycles and their derivatives are summarized and systematized. The relationship between the structure of azacrown compounds and their complexation behaviour towards metal cations is analyzed. The diversity of practical applications of azamacrocyclic derivatives in medicine, biology and analytical and organic chemistry, as well as for the design of molecular devices is demonstrated.
The bibliography includes 307 references.
Keywords: azacrown compounds, macrocyclization, complex formation.
Funding agency Grant number
Russian Science Foundation 16-13-10226
Ministry of Education and Science of the Russian Federation
Received: 29.07.2019
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: A. D. Zubenko, O. A. Fedorova, “Aromatic and heteroaromatic azacrown compounds: advantages and disadvantages of rigid macrocyclic ligands”, Russian Chem. Reviews, 89:7 (2020), 750–786
Citation in format AMSBIB
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\by A.~D.~Zubenko, O.~A.~Fedorova
\paper Aromatic and heteroaromatic azacrown compounds: advantages and disadvantages of rigid macrocyclic ligands
\jour Russian Chem. Reviews
\yr 2020
\vol 89
\issue 7
\pages 750--786
\mathnet{http://mi.mathnet.ru/eng/rcr4301}
\crossref{https://doi.org/10.1070/RCR4913}
\adsnasa{https://adsabs.harvard.edu/cgi-bin/bib_query?2020RuCRv..89..750Z}
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\elib{https://elibrary.ru/item.asp?id=45436227}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-85088502567}
Linking options:
  • https://www.mathnet.ru/eng/rcr4301
  • https://doi.org/10.1070/RCR4913
  • https://www.mathnet.ru/eng/rcr/v89/i7/p750
    • This publication is cited in the following 16 articles:
    1. Anastasia D. Zubenko, Anna V. Pashanova, Sofia P. Mosaleva, Ekaterina Y. Chernikova, Valentina A. Karnoukhova, Ivan V. Fedyanin, Bayirta V. Egorova, Anna A. Shchukina, Yury V. Fedorov, Olga A. Fedorova, Inorg. Chem., 2024  crossref
    2. L. I. Belen’kii, G. A. Gazieva, Yu. B. Evdokimenkova, N. O. Soboleva, Advances in Heterocyclic Chemistry, 139, 2023, 201  crossref
    3. L. S. Zamurueva, B. V. Egorova, I. S. Ikonnikova, A. D. Zubenko, A. V. Pashanova, V. A. Karnoukhova, A. A. Mitrofanov, A. L. Trigub, A. A. Moiseeva, A. B. Priselkova, O. A. Fedorova, S. N. Kalmykov, Dalton Trans., 52:23 (2023), 8092  crossref
    4. A. A. Fesenko, A. D Shutalev, Beilstein J. Org. Chem., 19 (2023), 1728  crossref
    5. P. Hermann, J. Kotek, V. Kubíček, Comprehensive Heterocyclic Chemistry IV, 2022, 591  crossref
    6. G. R. Delpiano, A. Garau, V. Lippolis, J. I. Lachowicz, A. Salis, Dalton Trans., 51:32 (2022), 12271  crossref
    7. M. K. Rofouei, J. B. Ghasemi, L. Arjomandi-Behzad, H. Behnejad, Journal of Molecular Liquids, 357 (2022), 119145  crossref
    8. S. D. Tokarev, A. Botezatu, A. V. Khoroshutin, Yu. V. Fedorov, O. A. Fedorova, Mendeleev Communications, 32:3 (2022), 367  crossref
    9. A. A. Fesenko, A. D. Shutalev, Org. Biomol. Chem., 20:22 (2022), 4569  crossref
    10. P. Vezse, B. Benda, A. Fekete, Á. Golcs, T. Tóth, P. Huszthy, Molecules, 27:9 (2022), 2838  crossref
    11. P. A. Panchenko, Yu. V. Fedorov, A. S. Polyakova, O. A. Fedorova, Mendeleev Commun., 31:4 (2021), 517–519  crossref  isi  scopus
    12. B. V. Egorova, T. P. Kalmykova, A. D. Zubenko, A. A. Shchukina, V. A. Karnoukhova, D. V. Likhosherstova, A. B. Priselkova, Yu. V. Fedorov, O. A. Fedorova, S. N. Kalmykov, Eur. J. Inorg. Chem., 2021:45 (2021), 4700–4709  crossref  isi
    13. I. L. Eremenko, F. M. Dolgushin, Russ. Chem. Rev., 90:12 (2021), 1493–1519  mathnet  crossref  isi
    14. A. D. Averin, A. N. Uglov, G. A. Zubrienko, A. S. Abel, A. K. Buryak, I. P. Beletskaya, Russ. Chem. Bull., 70:11 (2021), 2164–2179  crossref  isi  scopus
    15. Anastasia D. Zubenko, Bayirta V. Egorova, Lyubov S. Zamurueva, Stepan N. Kalmykov, Olga A. Fedorova, Mendeleev Communications, 31:2 (2021), 194  crossref
    16. Charles N. Moorefield, George R. Newkome, Progress in Heterocyclic Chemistry, 33, 2021, 583  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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