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Reduction of halogenated ketones with magnesium haloalkoxides

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The degree of thermal stability of magnesium haloalkoxycarbinolates containing thienyl groups and dichloro-, trichloro-, and trifluoromethyl groups was explained. The effect of substituents in the thienyl group on the stability of the magnesium haloalkoxycarbinolates was studied.

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Authors and Affiliations

  1. A. M. Gorkii Perm State University, USSR

    I. I. Lapkin, E. V. Dormidontova, Yu. P. Dormidontov, P. A. Sentebov & L. D. Parfenova

Authors
  1. I. I. Lapkin
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  2. E. V. Dormidontova
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  3. Yu. P. Dormidontov
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  4. P. A. Sentebov
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  5. L. D. Parfenova
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Additional information

Communication XXXV from the series “Reaction of Metal Haloalkoxides;” see [1] for communication XXIV.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1171–1174, September, 1971.

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Lapkin, I.I., Dormidontova, E.V., Dormidontov, Y.P. et al. Reduction of halogenated ketones with magnesium haloalkoxides. Chem Heterocycl Compd 7, 1101–1104 (1971). https://doi.org/10.1007/BF00510010

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  • DOI: https://doi.org/10.1007/BF00510010

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