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Condensation of 3,3-dichloroacrolein with cyclic ketones and cyclization of the condensation products to 2H-pyran-2-one derivatives

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    In the reaction of 3,3-dichloroacrolein with cyclic ketones, 2∶1 condensation products are formed.

  2. 2.

    The products of the cyclization of 3,3-dichloroacrolein with cyclic ketones are readily cyclized in an acid medium into the corresponding 2H-pyran-2-one derivatives.

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Literature cited

  1. L. I. Zakharkin and L. P. Sorokina, Izv. AN SSSR, Otd. khim. n.1958, 1445.

  2. A. Roedig, R. Marger, and S. Schödel, Chem. Ber.93, 2294 (1960).

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Authors and Affiliations

  1. Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, USSR

    L. I. Zakharkin & L. P. Sorokina

Authors
  1. L. I. Zakharkin
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  2. L. P. Sorokina
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Zakharkin, L.I., Sorokina, L.P. Condensation of 3,3-dichloroacrolein with cyclic ketones and cyclization of the condensation products to 2H-pyran-2-one derivatives. Russ Chem Bull 11, 264–266 (1962). https://doi.org/10.1007/BF00908030

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  • DOI: https://doi.org/10.1007/BF00908030

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