Abstract
The fragmentation pathways of 2-keto(thio)-6-methyl-5-carbethoxy(acetyl)-4-aryl-1,2,3,4-tetrahydropyrimidines were established using high resolution mass spectra and DADI spectra. An unusual rearrangement was observed, which involves cyclization of the aryl substituent in the 4 position with the oxygen of an ester group and elimination of a C2H5 radical.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 360–365, March, 1989.
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Stashenko, E.E., Zakharov, P.I., Pleshakov, V.G. et al. Mass spectrometric study of 2-keto(thio)tetrahydropyrimidine derivatives. Chem Heterocycl Compd 25, 301–305 (1989). https://doi.org/10.1007/BF00472390
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DOI: https://doi.org/10.1007/BF00472390