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Reactivity of Condensed Isoflavone Derivatives for Hydrazine

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Chemistry of Natural Compounds Aims and scope

Recyclization by hydrazine of furo[3,2-b]pyrano[2,3-f]chromen-4-ones, dipyrano[2,3-b:2,3-f]chromen4-ones, and pyrano[2,3-a]xanthen-4-ones derived from natural isoflavonoids and their analogs was studied. The reaction was shown to proceed selectively with opening of the chromone ring. Several substituted 4-arylpyrazoles containing furo[3,2-b]chromen-5-ol, pyrano[2,3-b]chromen-6-ol, and xanthen-8-ol fragments were synthesized.

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Authors and Affiliations

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

    G. P. Mrug & M. S. Frasinyuk

  2. Taras Shevchenko Kiev National University, 64 Vladimirskaya St, Kiev, 01601, Ukraine

    N. V. Bondarenko

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

    S. P. Bondarenko

Authors
  1. G. P. Mrug
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  2. N. V. Bondarenko
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  3. S. P. Bondarenko
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  4. M. S. Frasinyuk
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Correspondence to M. S. Frasinyuk.

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Translated from Khimiya Prirodnykh Soedinenii, No. 4, July–August, 2018, pp. 554–558

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Mrug, G.P., Bondarenko, N.V., Bondarenko, S.P. et al. Reactivity of Condensed Isoflavone Derivatives for Hydrazine. Chem Nat Compd 54, 654–659 (2018). https://doi.org/10.1007/s10600-018-2439-3

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  • DOI: https://doi.org/10.1007/s10600-018-2439-3

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