Journal
CHEMICAL COMMUNICATIONS
Volume 50, Issue 98, Pages 15525-15528Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc07807a
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- Grants-in-Aid for Scientific Research [25750390] Funding Source: KAKEN
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Dibenzo[b,h][1,6]naphthyridines were synthesized in one pot by reacting 2-acetylaminobenzaldehyde with methyl ketones under basic conditions via four sequential condensation reactions. This method was also applied to the synthesis of 1,2-dihydroquinolines. 6-Methyl-1,6-dibenzonaphthyridinium triflates showed strong fluorescence, and the fluorescence intensities were changed upon intercalation into double-stranded DNA.
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