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Reduction of peroxide products of ozonolysis of cyclooctene by sebacic acid dihydrazide
- Authors: Yakovleva M.P.1, Kravchenko A.A.1, Saitov K.M.1, Nazarov I.S.1, Ishmuratova N.M.1, Ishmuratov G.Y.1
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Affiliations:
- Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
- Issue: Vol 61, No 2 (2025)
- Pages: 192-196
- Section: Articles
- URL: https://rjmseer.com/0514-7492/article/view/684332
- DOI: https://doi.org/10.31857/S0514749225020095
- EDN: https://elibrary.ru/DHEGAG
- ID: 684332
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Abstract
It was found that the reduction of ozonolysis peroxide of cyclooctene products by sebacic acid dihydrazide in solvents of various natures leads to the formation of three acyclic differently functionalized cyclooctene derivatives: in methanol – dimethyl 11,20-dioxo-9,10,21,22-tetraazatriacont-8E,22E-dienoic acid, in methylene chloride – 11,20-dioxo-9,10,21,22-tetraazatriacta-8E,22E-diene acid, in THF – natural cortic acid.
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About the authors
M. P. Yakovleva
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Author for correspondence.
Email: insect@anrb.ru
ORCID iD: 0000-0002-2932-7483
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
A. A. Kravchenko
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID iD: 0000-0002-9385-8713
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
K. M. Saitov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID iD: 0000-0002-5391-3941
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
I. S. Nazarov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID iD: 0000-0002-9107-347X
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
N. M. Ishmuratova
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID iD: 0000-0002-9114-1284
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
G. Y. Ishmuratov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID iD: 0000-0002-7549-1874
Russian Federation, prosp.Oktabrya, 71, Ufa, 450054
References
- Беляева Э.Р., Мясоедова Ю.В., Ишмуратова Н.М., Ишмуратов Г.Ю. Биоорган. хим. 2022, 48, 648–676. [Belyaeva E.R., Myasoedova Y.V., Ishmuratova N.M., Ishmuratov G.Y. Russ. J. Bioorg. Chem. 2022, 48, 1123–1150.] doi: 10.1134/S1068162022060085
- Ишмуратов Г.Ю., Мингалеева Г.Р., Яковлева М.П., Шаханова О.О., Муслухов Р.Р., Толстиков А.Г. ЖОрХ. 2011, 47, 1392–1400. [Ishmuratov G.Y., Mingaleeva G.R., Yakovleva M.P., Shakhanova O.O., Muslukhov R.R., Tolstikov A.G. Russ. J. Org. Chem. 2011, 47, 1410–1415.] doi: 10.1134/S1070428011090259
- Ишмуратов Г.Ю., Мингалеева Г.Р., Яковлева М.П., Муслухов Р.Р., Шаханова О.О., Вырыпаев Е.М., Толстиков А.Г. ЖОрХ, 2011, 47, 1386–1391. [Ishmuratov G.Y., Mingaleeva G.R., Yakovleva M.P., Shakhanova O.O., Vyrypaev E.M., Tolstikov A.G. Russ. J. Org. Chem. 2011, 47, 1410–1415.] doi: 10.1134/S1070428011090259
- Ишмуратов Г.Ю., Легостаева Ю.В., Боцман Л.П., Толстиков Г.А. ЖОрХ. 2010, 46, 1591–1617. [Ishmuratov G.Y., Legostaeva Y.V., Botsman L.P., Tolstikov G.A. Russ. J. Org. Chem. 2010, 46, 1593–1621.] doi: 10.1134/S1070428010110011
- Черница Б.В., Ершов А.Ю., Комарова Д.А., Якимович С.И., Пакалънис В.В., Зерова И.В., Лагода И.В., Шаманин В.В. ХГС, 2009, 1725–1727. [Chernitsa B.V., Ershov A.Yu., Komarova D.A., Yakimovich S.I., Pakal'nis V.V., Zerova I.V., Lagoda I.V., Shamanin V.V. Chem. Heterocycl. Compd. 2009, 45, 1388–1390.] doi: 10.1007/s10593-010-0437-x
- Легостаева Ю.В., Боцман Л.П., Назаров И.С., Талипова Г.Р., Баннова А.В., Козлова Г.Г., Ишмуратов Г.Ю., Вестник Башкирск. ун-та. 2015, 20, 43–49. [Legostaeva Yu.V., Bocman L.P., Nazarov I.S., Talipova G.R., Bannova A.V., Kozlova G.G., Ishmuratov G.Yu., Vestnik Bashkirsk. un-ta. 2015, 20, 43–49.]
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