Issue 98, 2014

One-pot synthesis of dibenzo[b,h][1,6]naphthyridines from 2-acetylaminobenzaldehyde: application to a fluorescent DNA-binding compound

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.

Graphical abstract: One-pot synthesis of dibenzo[b,h][1,6]naphthyridines from 2-acetylaminobenzaldehyde: application to a fluorescent DNA-binding compound

Supplementary files

Article information

Article type
Communication
Submitted
03 Oct 2014
Accepted
23 Oct 2014
First published
23 Oct 2014

Chem. Commun., 2014,50, 15525-15528

Author version available

One-pot synthesis of dibenzo[b,h][1,6]naphthyridines from 2-acetylaminobenzaldehyde: application to a fluorescent DNA-binding compound

K. Okuma, T. Koga, S. Ozaki, Y. Suzuki, K. Horigami, N. Nagahora, K. Shioji, M. Fukuda and M. Deshimaru, Chem. Commun., 2014, 50, 15525 DOI: 10.1039/C4CC07807A

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