Reduction of peroxide products of ozonolysis of cyclooctene by sebacic acid dihydrazide
- Autores: Yakovleva M.P.1, Kravchenko A.A.1, Saitov K.M.1, Nazarov I.S.1, Ishmuratova N.M.1, Ishmuratov G.Y.1
-
Afiliações:
- Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
- Edição: Volume 61, Nº 2 (2025)
- Páginas: 192-196
- Seção: Articles
- URL: https://hum-ecol.ru/0514-7492/article/view/684332
- DOI: https://doi.org/10.31857/S0514749225020095
- EDN: https://elibrary.ru/DHEGAG
- ID: 684332
Citar
Resumo
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.
Palavras-chave
Texto integral

Sobre autores
M. Yakovleva
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Autor responsável pela correspondência
Email: insect@anrb.ru
ORCID ID: 0000-0002-2932-7483
Rússia, prosp.Oktabrya, 71, Ufa, 450054
A. Kravchenko
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID ID: 0000-0002-9385-8713
Rússia, prosp.Oktabrya, 71, Ufa, 450054
K. Saitov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID ID: 0000-0002-5391-3941
Rússia, prosp.Oktabrya, 71, Ufa, 450054
I. Nazarov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID ID: 0000-0002-9107-347X
Rússia, prosp.Oktabrya, 71, Ufa, 450054
N. Ishmuratova
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID ID: 0000-0002-9114-1284
Rússia, prosp.Oktabrya, 71, Ufa, 450054
G. Ishmuratov
Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences
Email: insect@anrb.ru
ORCID ID: 0000-0002-7549-1874
Rússia, prosp.Oktabrya, 71, Ufa, 450054
Bibliografia
- 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.]
Arquivos suplementares
