Reaction of 2-(ω-bromoalkylthio)-4,6-dimethylpyrimidines with some nucleophilic reagents

doi:10.1007/bf00954426

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Reaction of 2-(ω-bromoalkylthio)-4,6-dimethylpyrimidines with some nucleophilic reagents

Published 1982 · A. S. Mikhailov, N. G. Pashkurov, V. Reznik

Bulletin of the Academy of Sciences of the USSR, Division of chemical science

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Abstract

Conclusions1.The reaction of 2-(ω-bromoalkylthio)-4,6-dimethylpyrimidines with several nucleophilic reagents was studied under various conditions.2.Cyclic sulfonium or ammonium salts play a significant role in these transformations in the case of four methylene groups in the bromoalkyl group. The participation of these salts was supported by finding the products of their subsequent conversions.

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Cyclic sulfonium or ammonium salts play a significant role in the transformation of 2-(-bromoalkylthio)-4,6-dimethylpyrimidines with various nucleophilic reagents, supporting their participation through their subsequent conversions.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Reaction of 2-(ω-bromoalkylthio)-4,6-dimethylpyrimidines with some nucleophilic reagents

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