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Synthesis of 7-(N-12-Cytisinylpropoxy)Isoflavones

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Chemistry of Natural Compounds Aims and scope

The reactions of cytisine with isoflavone glycidyl ethers were investigated. A series of cytisine–isoflavone conjugates were regioselectively synthesized via opening the oxirane ring by cytisine.

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Authors and Affiliations

  1. National University of Food Technologies, 68 Vladimirskaya St., Kiev, 01601, Ukraine

    S. P. Bondarenko, O. G. Makarenko & M. S. Frasinyuk

  2. S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan

    V. I. Vinogradova

  3. V. P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St, Kiev, 02094, Ukraine

    M. S. Frasinyuk

Authors
  1. S. P. Bondarenko
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  2. O. G. Makarenko
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  3. V. I. Vinogradova
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  4. M. S. Frasinyuk
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Corresponding author

Correspondence to S. P. Bondarenko.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 6, November–December, 2020, pp. 895–897.

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Bondarenko, S.P., Makarenko, O.G., Vinogradova, V.I. et al. Synthesis of 7-(N-12-Cytisinylpropoxy)Isoflavones. Chem Nat Compd 56, 1040–1043 (2020). https://doi.org/10.1007/s10600-020-03222-9

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  • DOI: https://doi.org/10.1007/s10600-020-03222-9

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