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Russian Chemical Reviews, 1998, Volume 67, Issue 4, Pages 263–278
DOI: https://doi.org/10.1070/RC1998v067n04ABEH000355
(Mi rcr1400)
 

This article is cited in 14 scientific papers (total in 14 papers)

Epoxidation of substituted norbornenes. Stereochemical aspects and accompanying intramolecular transformations

L. I. Kasyan

Dnepropetrovsk State University
Abstract: Traditional and new procedures for epoxidation of substituted norbornenes are described. The stereochemistry of this reaction and the influence of substituents on the reactivity of the substrate are analysed. The molecular rearrangements and heterocyclisation reactions that can accompany epoxidation are considered; examples of selective attack of oxidants at one of the double bonds in norbornenes containing an unsaturated substituent and also at a multiple bond in some polycyclic di- and triene systems are given. The bibliography includes 252 references.
Received: 28.02.1997
Bibliographic databases:
Document Type: Article
UDC: 547.422:547.551
Language: English
Original paper language: Russian


Citation: L. I. Kasyan, “Epoxidation of substituted norbornenes. Stereochemical aspects and accompanying intramolecular transformations”, Usp. Khim., 67:4 (1998), 299–316; Russian Chem. Reviews, 67:4 (1998), 263–278
Linking options:
  • https://www.mathnet.ru/eng/rcr1400
  • https://doi.org/10.1070/RC1998v067n04ABEH000355
  • https://www.mathnet.ru/eng/rcr/v67/i4/p299
  • This publication is cited in the following 14 articles:
    1. S. A. Durakov, A. A. Kolobov, V. R. Flid, Fine Chem. Technol., 17:4 (2022), 275  crossref
    2. H. M. Alimardanov, F. M. Veliyeva, N. I. Garibov, E. S. Musayeva, Russ J Appl Chem, 93:5 (2020), 729  crossref
    3. Makhmudova L.A., Pet. Chem., 59:2 (2019), 174–179  crossref  isi
    4. Aliyeva I L., Efendiyeva L.M., Babanly N.N., Guliyev A.D., Abbasov V.M., Process. Petrochem. Oil Refin., 20:4 (2019), 389–400  isi
    5. Alimardanov Kh.M., Sadygov O.A., Garibov N.I., Dadashova N.R., Almardanova M.B., Kuliev A.D., Pet. Chem., 57:5 (2017), 415–423  crossref  isi  scopus
    6. Resende Gabriela da Costa, Alvarenga E.S., Magn. Reson. Chem., 54:12 (2016), 968–974  crossref  isi  scopus
    7. Garibov N.I., Process. Petrochem. Oil Refin., 17:4 (2016), 292–301  isi
    8. Samiran Bhattacharjee, Trevor J. Dines, James A. Anderson, J. Phys. Chem. C, 112:36 (2008), 14124  crossref
    9. Lilija Kasyan, Andrey Kasyan, Igor Tarabara, Sergiy Okovytyy, Elena Golodayeva, Andrey Tokar, Yevgeniy Podolyan, Open Chemistry, 6:2 (2008), 161  crossref
    10. Lilija I. Kasyan, Igor N. Tarabara, Andrey O. Kasyan, Sergiy I. Okovytyy, Andrey V. Tokar, Svetlana V. Shishkina, Oleg V. Shishkin, Tetrahedron, 63:8 (2007), 1790  crossref
    11. Günter Haufe, Dörthe Wölker, Eur J Org Chem, 2003:11 (2003), 2159  crossref
    12. L.I. Belen'kii, N.D. Kruchkovskaya, V.N. Gramenitskaya, Advances in Heterocyclic Chemistry, 79, 2001, 199  crossref
    13. Amalia Asouti, Lazaros P Hadjiarapoglou, Tetrahedron Letters, 41:4 (2000), 539  crossref
    14. L. I. KASYAN, ChemInform, 29:36 (1998)  crossref
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