V. V. Shereshovets, S. L. Khursan, V. D. Komissarov, G. A. Tolstikov, “Organic hydrotrioxides”, Usp. Khim., 70:2 (2001), 123–148; Russian Chem. Reviews, 70:2 (2001), 105

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Russian Chemical Reviews, 2001, Volume 70, Issue 2, Pages 105–129
DOI: https://doi.org/10.1070/RC2001v070n02ABEH000622 (Mi rcr739)

This article is cited in 27 scientific papers (total in 27 papers)

Organic hydrotrioxides

V. V. Shereshovets^a, S. L. Khursan^b, V. D. Komissarov^b, G. A. Tolstikov^c

^a Institute of Organic Chemistry, Ufa Scientific Centre of RAS
^b Bashkir State University, Ufa
^c N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistryof the Siberian Branch of Russian Academy of Sciences

English full-text Citations (27) Russian version article

DOI: https://doi.org/10.1070/RC2001v070n02ABEH000622

Abstract: The results of studies on the synthesis, structure, thermochemistry and oxidising capacity of organic hydrotrioxides are generalised. Particular emphasis is placed on the analysis of thermal and catalytic decomposition of ROOOH and on generation of free radicals and singlet molecular oxygen. Problems concerning the mechanisms of formation and decomposition of organic hydrotrioxides are also considered. The bibliography includes 154 references.

Received: 28.08.2000

Bibliographic databases:

Document Type: Article

UDC: 541.124:541.127:546.214:547.39

Language: English

Original paper language: Russian

Citation: V. V. Shereshovets, S. L. Khursan, V. D. Komissarov, G. A. Tolstikov, “Organic hydrotrioxides”, Usp. Khim., 70:2 (2001), 123–148; Russian Chem. Reviews, 70:2 (2001), 105–129

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https://doi.org/10.1070/RC2001v070n02ABEH000622

https://www.mathnet.ru/eng/rcr/v70/i2/p123

This publication is cited in the following 27 articles:

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S. A. Grabovskiy, Russ J Gen Chem, 92:8 (2022), 1443
Khalitova L.R., Grabovskii S.A., Kabal'nova N.N., High Energy Chem., 53:6 (2019), 435–437
Khalitova L.R., Antipin A.V., Grabovskii S.A., Kabal'nova N.N., High Energy Chem., 52:5 (2018), 446–448
Audran G., Marque S.R.A., Santelli M., Tetrahedron, 74:43 (2018), 6221–6261
Wurmel J., Simmie J.M., J. Phys. Chem. A, 121:42 (2017), 8053–8060
J. Würmel, J. M. Simmie, J. Phys. Chem. A, 121:42 (2017), 8053
Grabovskiy S.A., Khalitova L.R., Fedorova A.V., Lobov A.N., Rol'nik L.Z., Kabal'nova N.N., Russ. Chem. Bull., 65:2 (2016), 464–468
Reisi-Vanani A., Shahrokh L., Kokhdan S.N., Comput. Theor. Chem., 1051 (2015), 72–78
Khalitova L.R. Grabovskiy S.A. Antipin A.V. Spirikhin L.V. Kabal'nova N.N., Russ. J. Organ. Chem., 51:12 (2015), 1710–1716
Strle G., Cerkovnik J., Angew. Chem.-Int. Edit., 54:34 (2015), 9917–9920
Gregor Strle, Janez Cerkovnik, Angewandte Chemie, 127:34 (2015), 10055
Ono K., Akaike T., Sawa T., Kumagai Y., Wink D.A., Tantillo D.J., Hobbs A.J., Nagy P., Xian M., Lin J., Fukuto J.M., Free Radic. Biol. Med., 77 (2014), 82–94
Rossella Mello, María Elena González Núñez, Patai's Chemistry of Functional Groups, 2014, 1
Sergey L. Khursan, Patai's Chemistry of Functional Groups, 2014, 1
Janez Cerkovnik, Božo Plesničar, Chem. Rev., 113:10 (2013), 7930
V. N. Odinokov, Russ Chem Bull, 61:7 (2012), 1391
Céline Reynaud, Michel Giorgi, Henri Doucet, Maurice Santelli, Tetrahedron, 66:23 (2010), 4101
R. G. Savchenko, Ya. R. Urazaeva, R. V. Shafikov, V. N. Odinokov, Russ J Org Chem, 45:8 (2009), 1149
Rimma G. Savchenko, Yana R. Urmanova, Ruslan V. Shafikov, Svetlana R. Afon'kina, Leonard M. Khalilov, Victor N. Odinokov, Mendeleev Communications, 18:4 (2008), 191

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