Reduction of the Peroxide Products of Cyclooctene Ozonolysis with Sebacic Acid Dihydrazide

IF 0.8 4区化学 Q4 CHEMISTRY, ORGANIC

Russian Journal of Organic Chemistry Pub Date : 2025-04-15 DOI:10.1134/S1070428024604217

M. P. Yakovleva, A. A. Kravchenko, K. A. Saitov, I. S. Nazarov, N. M. Ishmuratova, G. Y. Ishmuratov

引用次数: 0

Abstract

The reduction with sebacic acid dihydrazide of the peroxide products of cyclooctene ozonolysis in different solvents leads, depending on the solvent, to three acyclic differently functionalized cyclooctene derivatives: methyl 11,20-dioxo-9,10,21,22-tetraazadocos-8E-enoic acid is formed in methanol, 11,20-dioxo-9,10,21,22-tetraazadocos-8E-enoic acid in methylene chloride, and natural cortic acid in THF.

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用癸二酸二酰肼还原环辛烯臭氧分解在不同溶剂中的过氧化物产物，根据溶剂的不同，会产生三种无环的不同官能化环辛烯衍生物：在甲醇中生成 11,20- 二氧代-9,10,21,22-四氮杂二十二烷-8E-烯酸甲酯，在二氯甲烷中生成 11,20- 二氧代-9,10,21,22-四氮杂二十二烷-8E-烯酸，在四氢呋喃中生成天然皮质酸。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Russian Journal of Organic Chemistry 化学-有机化学

CiteScore

1.40

自引率

25.00%

发文量

139

审稿时长

3-6 weeks

期刊介绍： Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.