Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties
M. Schmidtke, Jörg Reichert, Christoph Hoock
Molecules · 1999
doi:10.3390/41000264 (opens in a new tab)
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Abstract
Substitution of 4-methyl-[1,8]-naphthyridine in 2 and 7 position by alkylamines leads to highly fluorescent compounds. The arrangement of hydrogen donor and acceptor groups of these naphthyridines allows interactions with guanine and guanine cytosine base pairs. The described synthesis offers easy access to these small and stable fluorescent probes.
Abstract licence: CC BY
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