Synthesis and transformations of O-propargyl analogues of fusidic acid
- 作者: Salimova E.V.1, Golovnina D.A.1, Parfenova L.V.1
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隶属关系:
- Ufa Federal Research Center, Russian Academy of Sciences
- 期: 卷 61, 编号 3 (2025)
- 页面: 285-292
- 栏目: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://freezetech.ru/0514-7492/article/view/687806
- DOI: https://doi.org/10.31857/S0514749225030084
- EDN: https://elibrary.ru/EUCMMT
- ID: 687806
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详细
In continuation of the studies on synthetic modifications of fusidane triterpenoids, an O-propargyl fragment was introduced at the C3 atom of the fusidic acid methyl ester molecule and chemical transformations of the triple bond were carried out through reactions catalyzed by copper(I) salts to obtain an aminomethylene analogue, 1,2,3-triazole, and an aryl-substituted acetylene derivative.
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作者简介
E. Salimova
Ufa Federal Research Center, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: salimovaev@mail.ru
ORCID iD: 0000-0002-4328-5080
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075D. Golovnina
Ufa Federal Research Center, Russian Academy of Sciences
Email: salimovaev@mail.ru
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075L. Parfenova
Ufa Federal Research Center, Russian Academy of Sciences
Email: salimovaev@mail.ru
ORCID iD: 0000-0003-2816-2178
Institute of Petrochemistry and Catalysis
俄罗斯联邦, prosp. Oktyabrya, 141, Ufa, 450075参考
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