Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties

doi:10.3390/41000264

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Molecules 1999, 4(10), 264-271; doi:10.3390/41000264

Article

Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties

Christoph Hoock^1,* , Jörg Reichert² and M. Schmidtke²

¹ BYK-Gulden-Lomberg GmbH, D-78467 Konstanz, Germany ² Institute for Virology, University of Jena, Winzerlaerstr. 10, D-07745 Jena, Germany

* Author to whom correspondence should be addressed.

Received: 4 June 1999 / Accepted: 10 August 1999 / Published: 6 September 1999

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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.

Keywords: Naphthyridines; Fluorescence; Fluorescent probes

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MDPI and ACS Style

Hoock, C.; Reichert, J.; Schmidtke, M. Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties. Molecules 1999, 4, 264-271.

AMA Style

Hoock C., Reichert J., Schmidtke M. Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties. Molecules. 1999; 4(10):264-271.

Chicago/Turabian Style

Hoock, Christoph; Reichert, Jörg; Schmidtke, M. 1999. "Fluorescent 2,7-Dialkylamino-[1,8]-Naphthyridines: Preparation and Spectroscopic Properties." Molecules 4, no. 10: 264-271.

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