Reduction of peroxide products of ozonolysis of cyclooctene by sebacic acid dihydrazide

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

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.

全文:

受限制的访问

作者简介

M. Yakovleva

Ufa Institute of Chemistry, Ufa Research Center, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: insect@anrb.ru
ORCID iD: 0000-0002-2932-7483
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, prosp.Oktabrya, 71, Ufa, 450054

参考

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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.]

补充文件

附件文件
动作
1. JATS XML
2. Scheme 1

下载 (67KB)
3. Scheme 2

下载 (66KB)
4. Scheme 3

下载 (183KB)
5. Scheme 4

下载 (41KB)
6. Scheme 5

下载 (43KB)
7. Figure

下载 (115KB)

版权所有 © Russian Academy of Sciences, 2025