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Abstract <p>In continuation of our studies of modification of fusidane triterpenoids, <i>O</i>-propargyl fragment has been introduced at C<sup>3</sup> of fusidic acid methyl ester, and the resulting <i>O</i>-propargyl ether was subjected to copper(I)-catalyzed transformations to obtain aminomethyl, phenylacetylene, and 1,2,3-triazole derivatives.</p>

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Synthesis and Transformations of O-Propargyl Analogues of Fusidic Acid

  • 期刊论文

  • 发表日期：

    2025年3月1日

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  • E. V. Salimova,
  • D. A. Golovnina,
  • L. V. Parfenova

摘要

Abstract

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.