Synthesis and transformations of O-propargyl analogues of fusidic acid
- Autores: Salimova E.V.1, Golovnina D.A.1, Parfenova L.V.1
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							Afiliações: 
							
- Ufa Federal Research Center, Russian Academy of Sciences
 
 - Edição: Volume 61, Nº 3 (2025)
 - Páginas: 285-292
 - Seção: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
 - URL: https://kazanmedjournal.ru/0514-7492/article/view/687806
 - DOI: https://doi.org/10.31857/S0514749225030084
 - EDN: https://elibrary.ru/EUCMMT
 - ID: 687806
 
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Resumo
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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Sobre autores
E. Salimova
Ufa Federal Research Center, Russian Academy of Sciences
							Autor responsável pela correspondência
							Email: salimovaev@mail.ru
				                	ORCID ID: 0000-0002-4328-5080
				                																			                								
Institute of Petrochemistry and Catalysis
Rússia, prosp. Oktyabrya, 141, Ufa, 450075D. Golovnina
Ufa Federal Research Center, Russian Academy of Sciences
														Email: salimovaev@mail.ru
				                					                																			                								
Institute of Petrochemistry and Catalysis
Rússia, 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
Rússia, prosp. Oktyabrya, 141, Ufa, 450075Bibliografia
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