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Synthesis and Fluorescent Properties of Novel Isoquinoline Derivatives.

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.

SUBMITTER: Balewski L

PROVIDER: S-EPMC6891638 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Synthesis and Fluorescent Properties of Novel Isoquinoline Derivatives.

Balewski Łukasz Ł Sączewski Franciszek F Gdaniec Maria M Kornicka Anita A Cicha Karolina K Jalińska Aleksandra A

Molecules (Basel, Switzerland) 20191110 22

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, <i>N</i>,<i>N</i>-dimethylethylenediamine (DMEDA), and potassium carbonate. The structures of novel isoquinolin ...[more]

PMID: 31717684

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