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Dipolar [3+2]-Cycloaddition of Nitrones to 3-Alkoxycarbonyl- and 3-Pivaloyl-Substituted Hetareno[e]pyrrole-2,3-diones

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Abstract

[3+2]-Dipolar cycloaddition of 3-alkoxycarbonyl- and 3-pivaloyl-substituted hetareno[e]pyrrole-2,3-diones with diarylnitrones afforded alkaloid-like [1,2]oxazolo[5′,4′:2,3]pyrrolo[1,2-a]benzo[b]azines that attract interest for medicinal chemistry.

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Funding

This study was performed under financial support by the Russian Science Foundation (project no. 19-13-00290).

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Authors and Affiliations

  1. Perm State University, 614990, Perm, Russia

    A. A. Sabitov, E. E. Khramtsova, M. V. Dmitriev & A. N. Maslivets

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  1. A. A. Sabitov
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  2. E. E. Khramtsova
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  3. M. V. Dmitriev
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  4. A. N. Maslivets
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Corresponding author

Correspondence to A. N. Maslivets.

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The authors declare the absence of conflict of interest.

Additional information

Translated from Zhurnal Organicheskoi Khimii, 2022, Vol. 58, No. 3, pp. 270–280 https://doi.org/10.31857/S0514749222030053.

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Sabitov, A.A., Khramtsova, E.E., Dmitriev, M.V. et al. Dipolar [3+2]-Cycloaddition of Nitrones to 3-Alkoxycarbonyl- and 3-Pivaloyl-Substituted Hetareno[e]pyrrole-2,3-diones. Russ J Org Chem 58, 287–294 (2022). https://doi.org/10.1134/S1070428022030058

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