Abstract
α-(1-Cytosinyl)-γ-butyrolactone was obtained by condensation of bis(trimethylsilyl)cytosine with α-bromobutyrolactone. The reduction of α-(1-cytosinyl)-γ-butyrolactone with sodium borohydride gave N1-(1,4-dihydroxy-2-butyl)cytosine, the acylation of which with benzoyl chloride and subsequent partial hydrolysis gave N1-(1,4-dihydroxy-2-butyl)-N4-benzoylcytosine.
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See [1] for communication VIII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 694–698, May, 1975
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Giller, S.A., Zhuk, R.A., Berzinya, A.É. et al. Analogs of pyrimidine nucleosides. Chem Heterocycl Compd 11, 603–606 (1975). https://doi.org/10.1007/BF00480489
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DOI: https://doi.org/10.1007/BF00480489