Synthesis and Transformations of O-Propargyl Analogues of Fusidic Acid
In continuation of our studies of modification of fusidane triterpenoids, O-propargyl fragment has been introduced at C3 of fusidic acid methyl ester, and the resulting O-propargyl ether was subjected to copper(I)-catalyzed transformations to obtain aminomethyl, phenylacetylene, and 1,2,3-triazole derivatives.
Authors
- Е. В. Салимова (ORCID: https://orcid.org/0000-0002-4328-5080)
- Lyudmila V. Parfenova (ORCID: https://orcid.org/0000-0003-2816-2178)
- D. A. Golovnina
Institutions
- Ufa Institute of Chemistry (RU)
Publication Details
- Journal
- Russian Journal of Organic Chemistry
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1134/s1070428024604618
- Primary Topic
- Microbial Natural Products and Biosynthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00