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Russian Chemical Reviews, 1968, Volume 37, Issue 6, Pages 421–434
DOI: https://doi.org/10.1070/RC1968v037n06ABEH001650
(Mi rcr2176)
 

This article is cited in 17 scientific papers (total in 17 papers)

Oxidation of Sterically Hindered Phenols

L. M. Strigun, L. S. Vartanyan, N. M. Emanuel'

Institute of Chemical Physics of the USSR Academy of Sciences, Moscow
Abstract: The homolytic oxidation of sterically hindered phenols has been reviewed. The possible criteria of the reactivity of phenolic compounds, the properties of phenoxy-radicals–the primary products of oxidation by bound oxygen in non-polar media, and the kinetics of the reactions of phenoxy-radicals in the presence and absence of oxidants, have been discussed. Particular attention has been devoted to the oxidation of sterically hindered phenols in polar media by molecular oxygen, which exhibits a number of characteristic features. The bibliography comprises 84 references.
Document Type: Article
UDC: 547.563.1
Language: English
Original paper language: Russian


Citation: L. M. Strigun, L. S. Vartanyan, N. M. Emanuel', “Oxidation of Sterically Hindered Phenols”, Usp. Khim., 37:6 (1968), 969–997; Russian Chem. Reviews, 37:6 (1968), 421–434
Linking options:
  • https://www.mathnet.ru/eng/rcr2176
  • https://doi.org/10.1070/RC1968v037n06ABEH001650
  • https://www.mathnet.ru/eng/rcr/v37/i6/p969
  • This publication is cited in the following 17 articles:
    1. Jinhu Wang, Chunli Liu, Xuejing Liu, Linjun Shao, Xian‐Man Zhang, J of Physical Organic Chem, 32:5 (2019)  crossref
    2. H. Y. Hoang, R. M. Akhmadullin, F. Yu. Akhmadullina, R. K. Zakirov, A. G. Akhmadullina, A. S. Gazizov, Russ J Org Chem, 54:7 (2018), 1008  crossref
    3. Kh.I. Khoang, R.M. Akhmadullin, F. Yu. Akhmadullina, R. K. Zakirov, A.G. Akhmadullina, A. S. Gazizov, Zhurnal organicheskoi khimii, 2018, no. 7, 1006  crossref
    4. Hacı Ökkeş Demir, J of Applied Polymer Sci, 127:6 (2013), 5037  crossref
    5. Hacı Ökkeş Demir, Polym J, 44:7 (2012), 699  crossref
    6. S. Steenken, P. Neta, Patai's Chemistry of Functional Groups, 2009  crossref
    7. Veli T. Kasumov, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 57:3 (2001), 451  crossref
    8. A.V. Ragimov, B.A. Mamedov, Sh.I. Mustafaeva, Polymer, 30:10 (1989), 1851  crossref
    9. L. Jaulin, E. Chornet, Can J Chem Eng, 65:1 (1987), 64  crossref
    10. M. Sh. Vakhitova, B. I. Pantukh, G. A. Tolstikov, O. P. Yablonskii, R. B. Svitych, Russ Chem Bull, 36:8 (1987), 1675  crossref
    11. Karl Dimroth, Topics in Current Chemistry, 129, Photochemistry and Organic Synthesis, 1985, 99  crossref
    12. A.V. Ragimov, I.I. Ragimov, B.A. Mamedov, S.A. Guseinov, B.I. Liogon'kii, Polymer Science U.S.S.R., 24:10 (1982), 2434  crossref
    13. A. F. Pozharskii, A. A. Konstantinchenko, Chem Heterocycl Compd, 15:7 (1979), 787  crossref
    14. Eiichiro Manda, Bulletin of the Chemical Society of Japan, 47:11 (1974), 2727  crossref
    15. G. I. Zhungietu, G. A. Dragalina, G. N. Dorofeenko, Chem Heterocycl Compd, 9:1 (1973), 34  crossref
    16. Mihailo Lj. Mihailović, Živorad Čeković, PATAI'S Chemistry of Functional Groups, The Hydroxyl Group (1971), 1971, 505  crossref
    17. A. I. Prokof'ev, S. P. Solodovnikov, A. A. Volod'kin, V. V. Ershov, Russ Chem Bull, 20:5 (1971), 1021  crossref
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