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Halogenation of 1,5-Diketones

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Abstract

Published and experimental data of authors on halogenation of 1,5-diketones from acyclic (among them chalcogen-containing), semicyclic and bicyclic series resulting in formation of mono-, di-, tri-, and tertahalosubstituted 1,5-dioxo compounds, pyrylium halides, and their fused analogs or aroylfurans are reviewed.

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Authors and Affiliations

  1. Chernyshevsky Saratov State University, Saratov, 410071, Russia

    V. G. Kharchenko, O. V. Fedotova, N. V. Pchelintseva, L. I. Markova & D. A. Tsimbalenko

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  1. V. G. Kharchenko
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  2. O. V. Fedotova
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  3. N. V. Pchelintseva
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  4. L. I. Markova
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  5. D. A. Tsimbalenko
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Kharchenko, V.G., Fedotova, O.V., Pchelintseva, N.V. et al. Halogenation of 1,5-Diketones. Russian Journal of Organic Chemistry 39, 201–211 (2003). https://doi.org/10.1023/A:1025536102383

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