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.
CITATION STYLE
Johnston, C., Hardacre, C., & Migaud, M. E. (2021). Applications of Mechanochemistry for the Synthesis of DNA on Ionic Liquid Supports. Chemistry-Methods, 1(8), 382–388. https://doi.org/10.1002/cmtd.202100002
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