Paper
Suzuki–Miyaura Reactions of 2,7-Dichloro-1,8-naphthyridine
Published Jan 10, 2013 · Peter Ehlers, A. Petrosyan, T. Ghochikyan
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Abstract
2,7-Diaryl- and 2,7-dialkenyl-1,8-naphthyridines were prepared in high yields by Suzuki–Miyaura reactions of 2,7-dichloro-1,8-naphthyridines. While most of the products proved to be not or only weakly fluorescent, we observed a strong fluorescence in case of 2,7-bis(4-methoxyphenyl)-1,8-naphthyridine containing two electron-donating aryl groups.
Study Snapshot
Suzuki-Miyaura reactions of 2,7-dichloro-1,8-naphthyridine yield high yields of 2,7-diaryl-1,8-naphthyridine, with 2,7-bis(4-methoxyphenyl)-1,
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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