| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1372979 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages | 
Abstract
												Oxime bond formation has been applied to the preparation of oligonucleotides labeled with electrochemical ferrocene and viologen labels. Aminooxy functionalized ferrocene and viologen derivatives were prepared by a straightforward route and efficiently conjugated with aldehyde containing oligonucleotides either at 3′ or 5′ end. Both labels were found to not disturb the recognition properties of the oligonucleotide. The versatility of the method was further demonstrated by preparing bi-functionalized conjugates with a disulfide at 3′ end and an electrochemical label at 5′ end.
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											Authors
												Julie Moreau, Nabil Dendane, Bernd Schöllhorn, Nicolas Spinelli, Claire Fave, Eric Defrancq, 
											