Ring-chain tautomerism of 2-aryl-6-oxohexahydropyrimidine-4-carboxylic acid sodium salts
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作者:
A. Yu. Ershov
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
A. Yu. Ershov
D. G. Nasledov
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
D. G. Nasledov
K. V. Nasonova
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
K. V. Nasonova
K. V. Sezyavina
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
K. V. Sezyavina
T. V. Susarova
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
T. V. Susarova
I. V. Lagoda
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
I. V. Lagoda
V. V. Shamanin
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机构:Russian Academy of Sciences,Institute of Macromolecular Compounds
V. V. Shamanin
机构:
[1] Russian Academy of Sciences,Institute of Macromolecular Compounds
[2] Ministry of Defence of the Russian Federation,Research Test Medical and Biological Protection Center, State Research Test Institute of Military Medicine
It was shown by 1H and 13C NMR spectroscopy that the 2-aryl-6-oxohexahydropyrimidine-4-carboxylic acid sodium salts existed in D2O solution as a tautomeric mixture of cyclic and linear forms. The cyclic form consisted of two (2RS,4S)-stereoisomers, differing in the aryl substituent configuration at the pyrimidine ring C-2 atom.