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Russian Chemical Reviews, 2004, Volume 73, Issue 2, Pages 161–184
DOI: https://doi.org/10.1070/RC2004v073n02ABEH000788
(Mi rcr446)
 

This article is cited in 23 scientific papers (total in 23 papers)

Acetylenic derivatives of quinones

M. S. Shvartsberg, I. I. Barabanov, L. G. Fedenok

Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Science
Abstract: Methods for the preparation and various transformations of acetylenic derivatives of quinones, which are key intermediates in the synthesis of fused heterocyclic quinoid structures and some highly unsaturated compounds, are surveyed in detail.
Received: 23.10.2002
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian


Citation: M. S. Shvartsberg, I. I. Barabanov, L. G. Fedenok, “Acetylenic derivatives of quinones”, Usp. Khim., 73:2 (2004), 171–196; Russian Chem. Reviews, 73:2 (2004), 161–184
Linking options:
  • https://www.mathnet.ru/eng/rcr446
  • https://doi.org/10.1070/RC2004v073n02ABEH000788
  • https://www.mathnet.ru/eng/rcr/v73/i2/p171
  • This publication is cited in the following 23 articles:
    1. E. S. Trofimova, M. V. Zykova, M. G. Danilets, A. A. Ligacheva, E. Yu. Sherstoboev, N. S. Selivanova, L. A. Azarkina, A. M. Zhirkova, Yu. Zhang, I. V. Perminova, V. V. Zhdanov, M. V. Belousov, Bull Exp Biol Med, 177:1 (2024), 68  crossref
    2. S. F Vasilevsky, A. A Stepanov, Žurnal obŝej himii, 93:10 (2023), 1479  crossref
    3. S. F. Vasilevsky, A. A. Stepanov, Russ J Gen Chem, 93:10 (2023), 2417  crossref
    4. S. F. Vasilevskii, A. A. Stepanov, Russian Chem. Reviews, 91:1 (2022), RCR5020  mathnet  mathnet  crossref  isi  scopus
    5. Fedenok L. Dultsev F. Barabanov I. Polyakov N., Tetrahedron, 44 (2017), 6334–6340  crossref  isi  scopus
    6. Baranov D.S., Gatilov Yu.V., Mendeleev Commun., 26:4 (2016), 282–284  crossref  isi  scopus
    7. S. F. Vasilevskiy, D. S. Baranov, Chem Heterocycl Comp, 49:1 (2013), 140  crossref  isi  elib  scopus
    8. Silva M.G., Camara C.A., Silva T.M.S., Feitosa A.C.S., Meira A.S., Pessoa C., J. Braz. Chem. Soc., 24:9 (2013), 1420–U166  crossref  isi  elib  scopus
    9. Yasmin Akhtar, Murray B. Isman, Chi-Hoon Lee, Sang-Guei Lee, Hoi-Seon Lee, Industrial Crops and Products, 2011  crossref  isi  scopus
    10. Mitsuaki Yamashita, Kazunori Ueda, Koichi Sakaguchi, Akira Iida, Tetrahedron Letters, 2011  crossref  isi  scopus
    11. Gornostaev L.M., Arnold E.V., Lykova E.V., Sadoschenko M.V., Chem. Heterocycl. Compds., 46:6 (2010), 665–669  crossref  isi  scopus
    12. Shvartsberg M.S., Kolodina E.A., Lebedeva N.I., Fedenok L.G., Tetrahedron Lett., 50:49 (2009), 6769–6771  crossref  isi  elib  scopus
    13. Kolodina E.A., Shvartsberg M.S., Gritsan N.P., Mendeleev Commun., 18:6 (2008), 302–304  crossref  isi  elib  scopus
    14. Shvartsberg M.S., Kolodina E.A., Mendeleev Commun., 18:2 (2008), 109–111  crossref  isi  elib  scopus
    15. Alice L. Perez, G. Lamoureux, Bi Yun Zhen-Wu, Tetrahedron Letters, 48:23 (2007), 3995  crossref  isi  scopus
    16. S.F. Vasilevsky, L.M. Gornostaev, A.A. Stepanov, E.V. Arnold, I.V. Alabugin, Tetrahedron Letters, 48:10 (2007), 1867  crossref  isi  elib  scopus
    17. Belen'Kii L.I. Gramenitskaya V.N. Evdokimenkova Yu.B., Advances in Heterocyclic Chemistry, Vol 92, Adv. Heterocycl. Chem., 92, ed. Katritzky A., 2006, 145–258  crossref  isi  scopus
    18. N. V. Ivashkina, E. A. Yakovleva, I. D. Ivanchikova, A. A. Moroz, M. S. Shvartsberg, Russ Chem Bull, 54:6 (2005), 1509  crossref  isi  elib  scopus
    19. Walspurger S., Vasil'ev A., Sommer J., Pale P., Savechenkov P., Rudenko A., Russ. J. Organ. Chem., 41:10 (2005), 1485–1492  crossref  isi  elib  scopus
    20. M. S. Shvartsberg, I. I. Barabanov, L. G. Fedenok, ChemInform, 35:31 (2004)  crossref
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