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Synthesis of 7-Hydroxy-8-Methyl-4'-Methoxy-6-Formylisoflavone and Linear Hetarenochromones Based on It

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7-Hydroxy-8-methyl-4'-methoxy-6-formylisoflavone was synthesized from the 6-aminomethyl derivative of 7-hydroxychromone under modified Duff reaction conditions and underwent heterocyclization to form linear furo- and pyranochromones.

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Authors and Affiliations

  1. Taras Shevchenko National University of Kyiv, 64/13 Vladimirskaya St, Kyiv, 01601, Ukraine

    T. V. Shokol, N. V. Gorbulenko & V. P. Khilya

  2. V. P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St, Kyiv-94, 02094, Ukraine

    M. S. Frasinyuk

Authors
  1. T. V. Shokol
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  2. N. V. Gorbulenko
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  3. M. S. Frasinyuk
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  4. V. P. Khilya
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Corresponding author

Correspondence to T. V. Shokol.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 3, May–June, 2020, pp. 364–366.

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Shokol, T.V., Gorbulenko, N.V., Frasinyuk, M.S. et al. Synthesis of 7-Hydroxy-8-Methyl-4'-Methoxy-6-Formylisoflavone and Linear Hetarenochromones Based on It. Chem Nat Compd 56, 420–422 (2020). https://doi.org/10.1007/s10600-020-03052-9

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  • DOI: https://doi.org/10.1007/s10600-020-03052-9

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