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Russian Chemical Reviews, 2016, Volume 85, Issue 6, Pages 637–665
DOI: https://doi.org/10.1070/RCR4550
(Mi rcr4114)
 

This article is cited in 29 scientific papers (total in 29 papers)

Synthesis of (iso)quinoline, (iso)coumarin and (iso)chromene derivatives from acetylene compounds

D. S. Ryabukhina, A. V. Vasilyevab

a Saint Petersburg State University
b Saint-Petersburg State Forestry University
Abstract: Published data on the methods of synthesis of quinoline, isoquinoline, coumarin, isocoumarin, chromene and isochromene derivatives from acetylene compounds are summarized. The reactions catalyzed by metal complexes (Pd, Pt, Ru, Rh, Au, Ag, Ni, Cu, etc.) and transformations induced by various electrophilic reagents (Brynsted and Lewis acids) are considered. Moieties of the mentioned heterocyclic systems are present in many biologically active natural products and pharmaceutical agents. Besides, derivatives of these heterocycles are used in the manufacture of catalysts, dyes, perfumery and cosmetic products, corrosion inhibitors and so on.
The bibliography includes 211 references.
Received: 09.12.2014
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: D. S. Ryabukhin, A. V. Vasilyev, “Synthesis of (iso)quinoline, (iso)coumarin and (iso)chromene derivatives from acetylene compounds”, Russian Chem. Reviews, 85:6 (2016), 637–665
Citation in format AMSBIB
\Bibitem{RyaVas16}
\by D.~S.~Ryabukhin, A.~V.~Vasilyev
\paper Synthesis of (iso)quinoline, (iso)coumarin and (iso)chromene derivatives from acetylene compounds
\jour Russian Chem. Reviews
\yr 2016
\vol 85
\issue 6
\pages 637--665
\mathnet{http://mi.mathnet.ru/eng/rcr4114}
\crossref{https://doi.org/10.1070/RCR4550}
\adsnasa{https://adsabs.harvard.edu/cgi-bin/bib_query?2016RuCRv..85..637R}
\isi{https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Publons&SrcAuth=Publons_CEL&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=000379356100006}
\elib{https://elibrary.ru/item.asp?id=26003910}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84978516385}
Linking options:
  • https://www.mathnet.ru/eng/rcr4114
  • https://doi.org/10.1070/RCR4550
  • https://www.mathnet.ru/eng/rcr/v85/i6/p637
  • This publication is cited in the following 29 articles:
    1. A. Herlin Shamina, Vadivelan Ganesan, V. Bena Jothy, A. Manikandan, S. Muthu, Saleem Javed, Chemical Physics Impact, 8 (2024), 100394  crossref
    2. Devadkar Ajitrao Kisan, Ishita Paul, Soumyadip Dey, Abhijit Sau, Tarun K. Panda, Org. Biomol. Chem., 2024  crossref
    3. Marcelo H. R. Carvalho, Guilherme M. Martins, Giovanni W. Amarante, Pedro P. De Castro, Adv Synth Catal, 2024  crossref
    4. Shoele Bagheri‐Harsini, Ramin Ghorbani‐Vaghei, Azin Kharazmi, ChemistrySelect, 8:29 (2023)  crossref
    5. S. F Vasilevsky, A. A Stepanov, Zhurnal obschei khimii, 93:10 (2023), 1479  crossref
    6. S. F. Vasilevsky, A. A. Stepanov, Russ J Gen Chem, 93:10 (2023), 2417  crossref
    7. Addition Reactions with Unsaturated Hydrocarbons, 2022, 285  crossref
    8. Vladimir B. Kharitonov, Dmitry V. Muratov, Dmitry A. Loginov, Coordination Chemistry Reviews, 471 (2022), 214744  crossref
    9. Zhe Fu, Linjie Zhang, Sijin Hang, Shiyi Wang, Na Li, Xiaojing Sun, Zian Wang, Ruilong Sheng, Fang Wang, Wenhui Wu, Ruihua Guo, Polymers, 14:10 (2022), 2021  crossref
    10. Borisova M.A., Ryabukhin D.S., Ivanov A.Yu., Boyarskaya I.A., Spiridonova V Dar'ya, Kompanets M.O., Vasilyev A.V., Chem. Heterocycl. Compds., 57:10 (2021), 1007–1016  crossref  isi
    11. Zaitceva O., Beneteau V., Ryabukhin D.S., Louis B., Vasilyev A.V., Pale P., ChemCatChem, 12:1 (2020), 326–333  crossref  isi
    12. Gujjarappa R., Vodnala N., Malakar Ch.C., Adv. Synth. Catal., 362:22 (2020), 4896–4990  crossref  isi  scopus
    13. M. A. Borisova, D. S. Ryabukhin, A. V. Vasilyev, Chem. Heterocycl. Compds., 56:7 (2020), 964–967  crossref  isi  scopus
    14. V. N. Mikhaylov, A. O. Pavlov, Ya. V. Ogorodnov, D. V. Spiridonova, V. N. Sorokoumov, I. A. Balova, Chem. Heterocycl. Compds., 56:7 (2020), 915–922  crossref  isi  scopus
    15. J. S. Santos Neto, G. Zeni, Tetrahedron, 76:4 (2020), 130876  crossref  isi
    16. I. A. Balova, N. A. Danilkina, A. A. Vasileva, Russ. Chem. Rev., 89:1 (2020), 125–171  mathnet  crossref  isi  scopus
    17. O. Zaitceva, V. Beneteau, D. S. Ryabukhin, I. I. Eliseev, M. A. Kinzhalov, B. Louis, A. V. Vasilyev, P. Pale, Tetrahedron, 76:14 (2020), 131029  crossref  isi
    18. S. K. Nursahedova, A. V. Zerov, I. A. Boyarskaya, E. V. Grinenko, V. G. Nenajdenko, A. V. Vasilyev, Org. Biomol. Chem., 17:5 (2019), 1215–1224  crossref  isi  scopus
    19. W. Chen, Ch. Sun, Ya. Zhang, T. Hu, F. Zhu, X. Jiang, M. A. Abame, F. Yang, J. Suo, J. Shi, J. Shen, H. A. Aisa, J. Org. Chem., 84:13 (2019), 8702–8709  crossref  isi
    20. V. S. Moskvina, V. P. Khilya, Chem. Heterocycl. Compds., 55:4-5 (2019), 300–306  crossref  isi
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