Abstract
The standard methodology for the synthesis of oligonucleotides is the solid-phase method. Here, we report the first case of mechanochemistry being directly applied to synthesising a dinucleotide on a soluble support. While mechanochemistry eliminates the need to solubilise a supported oligomer in the solution phase for phosphoramidite coupling, the support still confers the benefit of being able to purify the product by precipitation or by simple liquid-liquid extractions as needed. Furthermore, this study also explores the use of mechanochemistry in the initial functionalisation of the ionic liquid support with a nucleoside monomer.
| Original language | English |
|---|---|
| Pages (from-to) | 382-388 |
| Number of pages | 7 |
| Journal | Chemistry-Methods |
| Volume | 1 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 2021 |
Keywords
- DNA synthesis
- ionic liquids
- mechanochemistry
- oligonucleotides
- soluble supports
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