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Russian Chemical Reviews, 1999, Volume 68, Issue 4, Pages 253–286
DOI: https://doi.org/10.1070/RC1999v068n04ABEH000463
(Mi rcr1458)
 

This article is cited in 30 scientific papers (total in 30 papers)

Dioxiranes: from oxidative transformations to chemiluminescence

V. P. Kazakov, A. I. Voloshin, D. V. Kazakov

Institute of Organic Chemistry, Ufa Scientific Centre of RAS
Abstract: Experimental data on the chemistry of a new class of highly effective oxidation reagents, dioxiranes, are summarised. The main methods used to generate dioxiranes and reactions in which dioxiranes have been proposed as intermediates are considered. The full notion about an important property of dioxiranes, i.e. the ability to oxidise rapidly, selectively and under mild conditions various classes of organic compounds (alkanes, alkenes, compounds containing heteroatoms, organometallic substrates, etc.) is given. Various aspects and mechanisms of these reactions are discussed. The attention is focused on the analysis of mechanisms of dioxirane decomposition in the absence of oxidisable substrates. One of the most attractive aspects of the dioxirane chemistry, chemiluminescence, is considered (the mechanisms of the generation of excited products during both thermal and catalytic decomposition and upon photochemical activation are discussed). The bibliography includes 401 references.
Received: 16.06.1998
Bibliographic databases:
Document Type: Article
UDC: 535.379:535.373.2:541.147.4:541.124:543.87:541.14:542.943
Language: English
Original paper language: Russian


Citation: V. P. Kazakov, A. I. Voloshin, D. V. Kazakov, “Dioxiranes: from oxidative transformations to chemiluminescence”, Usp. Khim., 68:4 (1999), 283–317; Russian Chem. Reviews, 68:4 (1999), 253–286
Linking options:
  • https://www.mathnet.ru/eng/rcr1458
  • https://doi.org/10.1070/RC1999v068n04ABEH000463
  • https://www.mathnet.ru/eng/rcr/v68/i4/p283
  • This publication is cited in the following 30 articles:
    1. Navjeet Kaur, 3-Membered Heterocycle Synthesis, 2024, 155  crossref
    2. A. L. Perkel, S. G. Voronina, Russ Chem Bull, 73:9 (2024), 2533  crossref
    3. Shuangqi Pi, Yanling Luo, Ya-Jun Liu, J. Phys. Chem. A, 126:38 (2022), 6604  crossref
    4. Khusnutdinova E.F., Kazakova O.B., Lobov A.N., Kukovinets O.S., Suponitsky K.Yu., Meyers C.B., Prichard M.N., Org. Biomol. Chem., 17:3 (2019), 585–597  crossref  isi  scopus
    5. Perkel A.L., Voronina S.G., Russ. Chem. Bull., 68:10 (2019), 1803–1820  crossref  isi
    6. Perkel A.L., Voronina S.G., Russ. Chem. Bull., 67:8 (2018), 1321–1329  crossref  isi  scopus
    7. Khusnutdinova El'mira F., Medvedeva N.I., Kazakov D.V., Kukovinets O.S., Lobov A.N., Suponitsky K.Yu., Kazakova O.B., Nat. Prod. Commun., 11:4 (2016), 449–452  isi
    8. El'mira F. Khusnutdinova, Natalya I. Medvedeva, Dmitri V. Kazakov, Olga S. Kukovinets, Alexander N. Lobov, Kirill Yu. Suponitsky, Oxana B. Kazakova, Natural Product Communications, 11:4 (2016), 1934578X1601100  crossref
    9. Izosimov I.N., J. Radioanal. Nucl. Chem., 304:1 (2015), 207–211  crossref  isi  elib  scopus
    10. Theodorou V., Skobridis K., Alivertis D., Gerothanassis I.P., J. Label. Compd. Radiopharm., 57:8 (2014), 481–508  crossref  isi  scopus
    11. Izosimov I.N., Firsin N.G., Gorshkov N.G., Nekhoroshkov S.N., Hyperfine Interact., 227:1-3 (2014), 271–281  crossref  isi  elib  scopus
    12. Ovchinnikov M.Yu., Kazakov D.V., Khursan S.L., Kinet. Catal., 53:1 (2012), 42–53  crossref  isi  elib  scopus
    13. Ovchinnikov M.Yu., Khursan S.L., Kazakov D.V., Russ. Chem. Bull., 60:1 (2011), 28–35  crossref  isi  elib  scopus
    14. D. V. Kazakov, M. Yu. Ovchinnikov, S. L. Khursan, High Energy Chem, 45:6 (2011), 459  crossref
    15. Kazakova O.B., Tretyakova E.V., Kukovinets O.S., Abdrakhmanova A.R., Kabalnova N.N., Kazakov D.V., Tolstikov G.A., Gubaidullin A.T., Tetrahedron Lett., 51:14 (2010), 1832–1835  crossref  isi  elib  scopus
    16. Ovchinnikov M.Yu., Khursan S.L., Kazakov D.V., Adam W., J. Photochem. Photobiol. A-Chem., 210:2-3 (2010), 100–107  crossref  isi  elib  scopus
    17. Waldemar Adam, Cong‐Gui Zhao, Kavitha Jakka, Oxidation of Organic Compounds by Dioxiranes, 2009, 311  crossref
    18. M. Roje, T. Portada, Comprehensive Heterocyclic Chemistry III, 2008, 641  crossref
    19. Waldemar Adam, Cong‐Gui Zhao, Kavitha Jakka, Organic Reactions, 2008, 1  crossref
    20. Dmitrii V. Kazakov, Farit E. Safarov, Valerii P. Kazakov, Reinhardt Schmidt, Mendeleev Communications, 18:5 (2008), 249  crossref
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