Issue 42, 2025

Synthesis, duplex-forming properties, and enzymatic resistance of oligonucleotides containing N-acylsulfonamide linkages

Abstract

We report the synthesis of (2-(N-acetylsulfamoyl)ethyl)carbamate (NAC)-linked thymidine dinucleotide via the sulfo-click reaction and its incorporation into DNA oligonucleotides. Thermal denaturation studies indicate modest destabilization at duplex ends (∼1 °C) and stronger effects in the middle (∼7 °C), while the NAC linkage provides complete resistance to nucleases.

Graphical abstract: Synthesis, duplex-forming properties, and enzymatic resistance of oligonucleotides containing N-acylsulfonamide linkages

Supplementary files

Article information

Article type
Communication
Submitted
26 Aug 2025
Accepted
29 Sep 2025
First published
29 Sep 2025

Org. Biomol. Chem., 2025,23, 9576-9581

Synthesis, duplex-forming properties, and enzymatic resistance of oligonucleotides containing N-acylsulfonamide linkages

R. Amador, C. Baraguey, G. Clavé and M. Smietana, Org. Biomol. Chem., 2025, 23, 9576 DOI: 10.1039/D5OB01382H

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