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Oxa-[3+3] annulation of 1H-benzo[f]chromene-2-carbaldehydes and 2-naphthols: synthesis of 7aH,15H-benzo[f]benzo[5,6]chromeno[2,3-b]chromenes

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Chemistry of Heterocyclic Compounds Aims and scope

A method for the preparation of polycondensed chromeno[2,3-b]chromenes was developed based on the formal [3+3] cycloaddition reaction between 1H-benzo[f]chromene-2-carbaldehydes and 2-naphthols. In the case of resorcinol, the bisannulation product formed with the participation of both hydroxy groups was isolated.

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This work was supported by the Russian Science Foundation (grant 19-13-00421) using the scientific equipment of the Center for Collective Use “Investigation of the physicochemical properties of substances and materials” of Samara State Technical University.

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Authors and Affiliations

  1. Samara State Technical University, 244 Molodogvardeyskaya St, Samara, 443100, Russia

    Irina А. Semenova, Vitaly А. Osyanin, Dmitry V. Osipov & Yuri N. Klimochkin

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  1. Irina А. Semenova
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  2. Vitaly А. Osyanin
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  3. Dmitry V. Osipov
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  4. Yuri N. Klimochkin
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Correspondence to Vitaly А. Osyanin.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2021, 57(6), 691–694

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Semenova, I.А., Osyanin, V.А., Osipov, D.V. et al. Oxa-[3+3] annulation of 1H-benzo[f]chromene-2-carbaldehydes and 2-naphthols: synthesis of 7aH,15H-benzo[f]benzo[5,6]chromeno[2,3-b]chromenes. Chem Heterocycl Comp 57, 691–694 (2021). https://doi.org/10.1007/s10593-021-02968-6

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