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Russian Chemical Reviews, 2021, Volume 90, Issue 3, Pages 395–417
DOI: https://doi.org/10.1070/RCR4988 (Mi rcr4338) 		 
This article is cited in 17 scientific papers (total in 17 papers)

Advances in the synthesis of heterocycles bearing an endocyclic urea moiety

A. V. Smolobochkin, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin

A. E. Arbuzov Institute of Organic and Physical Chemistry of Kazan Scientific Center of Russian Academy of Sciences
English full-text Citations (17) Russian version article
DOI: https://doi.org/10.1070/RCR4988
Abstract: The review systematizes and summarizes data on the synthesis of structurally diverse cyclic ureas published over the last 10 years. Saturated and unsaturated monocyclic ureas, as well as fused heterocycles containing one urea moiety, are considered. Data on the biological activity of selected compounds of this type are provided. The synthetic approaches to cyclic carbamides are classified in terms of the reaction type and the source of a carbonyl group.
The bibliography includes 235 references.
Received: 02.08.2020
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: A. V. Smolobochkin, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin, “Advances in the synthesis of heterocycles bearing an endocyclic urea moiety”, Russian Chem. Reviews, 90:3 (2021), 395–417
Citation in format AMSBIB
\Bibitem{SmoGazBur21}
\by A.~V.~Smolobochkin, A.~S.~Gazizov, A.~R.~Burilov, M.~A.~Pudovik, O.~G.~Sinyashin
\paper Advances in the synthesis of heterocycles bearing an endocyclic urea moiety
\jour Russian Chem. Reviews
\yr 2021
\vol 90
\issue 3
\pages 395--417
\mathnet{http://mi.mathnet.ru/eng/rcr4338}
\crossref{https://doi.org/10.1070/RCR4988}
\adsnasa{https://adsabs.harvard.edu/cgi-bin/bib_query?2021RuCRv..90..395S}
\isi{https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Publons&SrcAuth=Publons_CEL&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=000635530200004}
\elib{https://elibrary.ru/item.asp?id=46768741}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-85104256342}
Linking options:
  • https://www.mathnet.ru/eng/rcr4338
  • https://doi.org/10.1070/RCR4988
  • https://www.mathnet.ru/eng/rcr/v90/i3/p395
    • This publication is cited in the following 17 articles:
    1. Noureddine Benharkat, Fayssal Triki Baara, Abdelkader Chouaih, Şehriman Atalay, Muhittin Aygün, Nour El Houda Belkafouf, Necmi Dege, Mohamed Hadj Mortada Belhachemi, Ayada Djafri, Nourdine Boukabcha, ChemistrySelect, 10:1 (2025)  crossref
    2. Goncagül Serdaroğlu, Nesimi Uludag, Sümeyya Serin, Journal of Molecular Liquids, 423 (2025), 126989  crossref
    3. Pedro S. Beck, Arthur G. Leitão, Yasmin B. Santana, José R. Correa, Carime V. S. Rodrigues, Daniel F. S. Machado, Guilherme D. R. Matos, Luciana M. Ramos, Claudia C. Gatto, Sarah C. C. Oliveira, Carlos K. Z. Andrade, Brenno A. D. Neto, Org. Biomol. Chem., 2024  crossref
    4. Divya Chauhan, Harish Kumar Chopra, Surendra Kumar Nayak, COS, 21:1 (2024), 78  crossref
    5. Leonid I. Belen'kii, Galina A. Gazieva, Yulia B. Evdokimenkova, Natalya O. Soboleva, Advances in Heterocyclic Chemistry, 142, 2024, 139  crossref
    6. Yu. M. Sadykova, A. V. Smolobochkin, R. A. Turmanov, A. V. Zalaltdinova, A. S. Gazizov, M. A. Pudovik, A. R. Burilov, Russ J Gen Chem, 94:7 (2024), 1625  crossref
    7. Andrey Smolobochkin, Almir Gazizov, Nurbol Appazov, Oleg Sinyashin, Alexander Burilov, IJMS, 25:20 (2024), 11158  crossref
    8. V. V. Semenov, N. V. Zolotareva, B. I. Petrov, N. M. Lazarev, E. V. Baranov, Russ J Coord Chem, 50:10 (2024), 817  crossref
    9. M. A. Raza, K. Javaid, U. Farwa, A. Javaid, M. Yaseen, J. K. Maurin, A. Budzianowski, B. Iqbal, S. Ibrahim, Journal of Molecular Structure, 1271 (2023), 133989  crossref
    10. A. V. Smolobochkin, A. S. Gazizov, Chem. Heterocycl. Comp., 59:4-5 (2023), 237  crossref
    11. A. V. Smolobochkin, L. J. Yakhshilikova, T. S. Rizbayeva, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, Russ J Gen Chem, 93:3 (2023), 495  crossref  crossref
    12. A. V. Smolobochkin, E. A. Kuznetsova, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, Russ J Gen Chem, 93:6 (2023), 1322  crossref  crossref
    13. A. Smolobochkin, A. Gazizov, A. Burilov, M. Pudovik, Helv. Chim. Acta, 105:1 (2022), e2100158  crossref  isi  scopus
    14. A.. V. Smolobochkin, A. S. Gazizov, L. J. Yakhshilikova, N. A. Sidlyaruk, A. R. Khamatgalimov, A. R. Burilov, M. A. Pudovik, Tetrahedron, 120 (2022), 132874  crossref
    15. Gazizov A.S. Smolobochkin A.V. Kuznetsova E.A. Abdullaeva D.S. Burilov A.R. Pudovik M.A. Voloshina A.D. Syakaev V.V. Lyubina A.P. Amerhanova S.K. Voronina J.K., Molecules, 26:15 (2021), 4432  crossref  isi
    16. Matheny J.P., Aksenov A.V., Rubin M., Russ. Chem. Bull., 70:6 (2021), 1046–1066  crossref  isi
    17. Kibardina L.K., Trifonov V A., Dobrynin A.B., Pudovik M.A., Burilov A.R., Voloshina A.D., Strelnik A.G., Gazizov A.S., Mendeleev Commun., 31:5 (2021), 664–666  crossref  isi
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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