Issue 5, 2009

Synthesis and electrochemical studies of an anthraquinone-conjugated nucleoside and derived oligonucleotides

Abstract

The synthesis of a 2′-deoxyuridine nucleoside linked to an anthraquinone moiety, and its incorporation into oligonucleotides are described, including a facile oxidative demethylation with phenyliodine(III) bis(trifluoroacetate) to reveal the anthraquinone motif. Furthermore, some useful physical and electrochemical properties of the obtained oligonucleotide are also reported, which allow its principal use in electrochemical DNA assays.

Graphical abstract: Synthesis and electrochemical studies of an anthraquinone-conjugated nucleoside and derived oligonucleotides

Supplementary files

Article information

Article type
Paper
Submitted
25 Sep 2008
Accepted
18 Nov 2008
First published
23 Jan 2009

Org. Biomol. Chem., 2009,7, 905-908

Synthesis and electrochemical studies of an anthraquinone-conjugated nucleoside and derived oligonucleotides

M. F. Jacobsen, E. E. Ferapontova and K. V. Gothelf, Org. Biomol. Chem., 2009, 7, 905 DOI: 10.1039/B816820B

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