Paper
Synthesis and reactivity of bis(cycloamidinium-2-yl)alkane bromide tribromides, brominating agents and tectons for molecular engineering
Published Apr 11, 2008 · D. Długosz, M. Pach, Anna Zabrzeńska
Monatshefte für Chemie - Chemical Monthly
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Abstract
Bis(cycloamidine-2-yl)alkanes easily form bromide tribromide salts in the reduction-oxidation processes with bromine. Bis(tetrahydroimidazolium-2-yl)ethane and bis(hexahydropyrimidinium-2-yl)-ethane bromide tribromides are such new convenient brominating agents for aromatic amides in chemo- and regioselective electrophilic substitutions and α-bromination reactions.
Study Snapshot
Bis(cycloamidine-2-yl)alkane bromide tribromides are promising brominating agents for aromatic amides in chemo- and regioselective electrophilic substitutions and -bromination reactions.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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