Abstract
2,3-Asyridinylcarvone was synthesized from epoxycarvone through the stages of regio- and stereoselective opening of the epoxy ring under the action of NaN3 in methanolic NH4Cl followed by treatment with PPh3.
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ACKNOWLEDGMENTS
The spectral part of the studies and theoretical calculations were carried out using the equipment of the Central Collective Use Center “Khimiya” of the Ufa Institute of Chemistry of the Ural Federal Research Center of the Russian Academy of Sciences.
Funding
The work was performed by state assignment no. 122031400261-4 and financially supported by the Russian Foundation for Basic Research (project no. 20-33-90039 Graduate Students).
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Translated from Zhurnal Organicheskoi Khimii, 2022, Vol. 58, No. 5, pp. 548–550 https://doi.org/10.31857/S0514749222050135.
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Selezneva, N.K., Sunagatullina, G.R., Valiullina, Z.R. et al. Synthesis of the 2,3-Asyridinyl Derivative of d-Carvone. Russ J Org Chem 58, 724–726 (2022). https://doi.org/10.1134/S107042802205013X
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DOI: https://doi.org/10.1134/S107042802205013X