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Updated: Mar 28, 2026

Chemical Triphosphorylation of Oligonucleotides
Published on: June 2, 2022
Preparation of a disulfide-linked precipitative soluble support for solution-phase synthesis of trimeric
Amit M Jabgunde1, Alejandro Gimenez Molina2, Pasi Virta2
1Department of Chemistry, University of Turku, FIN-20014 Turku, Finland ; current address: Rega Institute for Medical Research, Minderbroedersstraat 10, KU Leuven, 3000- Leuven, Belgium.
Abstract:
The preparation of a disulfide-tethered precipitative soluble support and its use for solution-phase synthesis of trimeric oligodeoxyribonucleotide 3´-(2-chlorophenylphosphate) building blocks is described. To obtain the building blocks, N-acyl protected 2´-deoxy-5´-O-(4,4´-dimethoxytrityl)ribonucleosides were phosphorylated with bis(benzotriazol-1-yl) 2-chlorophenyl phosphate. The "outdated" phosphotriester strategy, based on coupling of P(V) building blocks in conjunction with quantitative precipitation of the oligodeoxyribonucleotide with MeOH is applied. Subsequent release of the resulting phosphate and base-protected oligodeoxyribonucleotide trimer 3'-pTpdC(Bz)pdG(ibu)-5' as its 3'-(2-chlorophenyl phosphate) was achieved by reductive cleavage of the disulfide bond.
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