A new strategy enables oxidation-free, efficient oligonucleotide synthesis
Researchers have developed an oxidation-free approach to oligonucleotide synthesis using P(V)-fluoridates, enabling rapid coupling and automated synthesis. The new platform offers improved efficiency and stability compared to conventional methods.
SourceTokushima University·JournalJournal of the American Chemical Society·TypeExperimental study·DateJul 29, 2026