Paper
Synthesis and properties of 3,5-dibromo-4-oxo-2,2,6,6-tetramethylpiperidine-1-oxyl radical
Published 1992 · I. Zhukova, E. Kagan, V. Smirnov
Chemistry of Heterocyclic Compounds
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Abstract
Bromination of 1-hydroxy-4-oxo-2,2,6,6-tetramethylpiperidine gives 3,5-dibromo-1-hydroxy-4-oxo-2,2,6,6-tetramethylpiperidine hydrobromide. Oxidation of the latter generates 3,5-dibromo-4-oxo-2,2,6,6-tetramethylpiperdine-1-oxyl radical, which represents a convenient acylating spin trap.
Study Snapshot
3,5-dibromo-4-oxo-2,2,6,6-tetramethylpiperidine-1-oxyl radical is a convenient acylating spin trap for synthesis of cycloadducts and cycloadducts with a tetramethylpiperidine
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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