Synthesis and transformations of O-propargyl analogues of fusidic acid
- Authors: Salimova E.V.1, Golovnina D.A.1, Parfenova L.V.1
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Affiliations:
- Ufa Federal Research Center, Russian Academy of Sciences
- Issue: Vol 61, No 3 (2025)
- Pages: 285-292
- Section: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://bioethicsjournal.ru/0514-7492/article/view/687806
- DOI: https://doi.org/10.31857/S0514749225030084
- EDN: https://elibrary.ru/EUCMMT
- ID: 687806
Cite item
Abstract
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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About the authors
E. V. Salimova
Ufa Federal Research Center, Russian Academy of Sciences
Author for correspondence.
Email: salimovaev@mail.ru
ORCID iD: 0000-0002-4328-5080
Institute of Petrochemistry and Catalysis
Russian Federation, prosp. Oktyabrya, 141, Ufa, 450075D. A. Golovnina
Ufa Federal Research Center, Russian Academy of Sciences
Email: salimovaev@mail.ru
Institute of Petrochemistry and Catalysis
Russian Federation, prosp. Oktyabrya, 141, Ufa, 450075L. V. Parfenova
Ufa Federal Research Center, Russian Academy of Sciences
Email: salimovaev@mail.ru
ORCID iD: 0000-0003-2816-2178
Institute of Petrochemistry and Catalysis
Russian Federation, prosp. Oktyabrya, 141, Ufa, 450075References
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