Abstract
The action of bromine and chlorine of phenacylpyrimidines yields a series of α-mono- and α,α′-dihalophenacylpyrimidines. IR, UV and PMR spectroscopy showed that, in contrast to the starting compounds, the monohalo derivatives exist in the keto form.
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Deceased.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 663–667, May, 1987.
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Semushkina, I.V., Zagulyaeva, O.A. & Mamaev, V.P. Halogenation of phenacylpyrimidines. Chem Heterocycl Compd 23, 550–553 (1987). https://doi.org/10.1007/BF00476386
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DOI: https://doi.org/10.1007/BF00476386