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Chem Commun (Camb) ; 50(98): 15525-8, 2014 Dec 21.
Article in English | MEDLINE | ID: mdl-25354542

ABSTRACT

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.


Subject(s)
DNA/chemistry , Fluorescent Dyes/chemical synthesis , Intercalating Agents/chemical synthesis , Naphthyridines/chemical synthesis , Benzaldehydes/chemistry , Fluorescence , Fluorescent Dyes/chemistry , Intercalating Agents/chemistry , Ketones/chemistry , Naphthyridines/chemistry , Quinolines/chemical synthesis , Quinolines/chemistry
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