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Synthesis of 5-Trimethylsilylethynyl-1,3,4-oxadiazoles

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Abstract

5-Trimethylsilylethynyl-2-R-1,3,4-oxadiazoles were synthesized for the first time by intramolecular cyclocondensation of unsymmetrical N-acyl-N'-(3-trimethylsilyl-2-propynoyl)hydrazines by the action of phosphoryl chloride.

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Authors and Affiliations

  1. Favorskii Irkutsk Institute of Chemistry, Siberian Division, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia

    M. M. Demina, G. I. Sarapulova, A. I. Borisova, L. I. Larina & A. S. Medvedeva

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  1. M. M. Demina
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  2. G. I. Sarapulova
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  3. A. I. Borisova
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  4. L. I. Larina
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  5. A. S. Medvedeva
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Demina, M.M., Sarapulova, G.I., Borisova, A.I. et al. Synthesis of 5-Trimethylsilylethynyl-1,3,4-oxadiazoles. Russian Journal of Organic Chemistry 39, 1522–1524 (2003). https://doi.org/10.1023/B:RUJO.0000010574.41923.83

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  • DOI: https://doi.org/10.1023/B:RUJO.0000010574.41923.83

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