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Updated: May 29, 2026

07:16
DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
Published on: February 9, 2024
Harnessing nature's insights: synthetic small molecules with peroxidase-mimicking DNAzyme properties
Loic Stefan1, Hai-Jun Xu, Claude P Gros
1Institut de Chimie Moléculaire de l'Université de Bourgogne (ICMUB), CNRS UMR5260, 9, Avenue Alain Savary, 21000 Dijon, France.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|September 16, 2011
Abstract
No abstract available in PubMed .
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The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.

