Paper
Nitroazines 11. Structure of products of transformation OF 6-nitroazolo-[1,5-a]pyrimidines under the influence of cyanoacetic ester
Published Dec 1, 1990 ยท V. Rusinov, T. L. Pilicheva, A. Tumashov
Chemistry of Heterocyclic Compounds
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Abstract
The interaction of 6-nitroazolo[1,5-a]pyrimidines with ethyl cyanoacetate is accompanied by transformation of the pyrimidine ring, forming derivatives of 2-azolylaminopyrimidine. The structure of the transformation products has been investigated in crystals and in solution.
Study Snapshot
The interaction of 6-nitroazolo[1,5-a]pyrimidines with ethyl cyanoacetate leads to transformation of the pyrimidine ring, forming 2-azolylaminopyrimidine derivatives in crystals and solution.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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