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Molecules. 2019 Nov 10;24(22). pii: E4070. doi: 10.3390/molecules24224070.

Synthesis and Fluorescent Properties of Novel Isoquinoline Derivatives.

Author information

1
Department of Chemical Technology of Drugs, Faculty of Pharmacy, Medical University of Gdańsk, 80-416 Gdańsk, Poland.
2
Faculty of Chemistry, Adam Mickiewicz University, 61-614 Poznań, Poland.

Abstract

Isoquinoline derivatives have attracted great interest for their wide biological and fluorescent properties. In the current study, we focused on the synthesis of a series of novel isoquinoline derivatives substituted at position 3 of the heteroaromatic ring. Compounds were obtained in a Goldberg-Ullmann-type coupling reaction with appropriate amides in the presence of copper(I) iodide, N,N-dimethylethylenediamine (DMEDA), and potassium carbonate. The structures of novel isoquinolines were confirmed by IR, NMR, and elemental analysis, as well as X-ray crystallography. In the course of our research work, the visible fluorescence of this class of compounds was observed. The above findings prompted us to investigate the optical properties of the selected compounds.

KEYWORDS:

X-ray crystallography; copper-catalyzed coupling; fluorescence; isoquinoline derivatives

PMID:
31717684
DOI:
10.3390/molecules24224070
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