Synthesis of novel pyrophosphorothiolate-linked dinucleoside cap analogues in a ball mill

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Abstract

Michaelis-Arbuzov reactions of S-aryl disulfide derivatives of 3′-thiothymidine or 5′-thioadenosine with tris(trimethylsilyl) phosphite proceeded in high yields to the corresponding phosphorothiolate monoesters. Subsequent hydrolytic desilylation and phosphate coupling were effected in one-pot using liquid-assisted grinding in a vibration ball mill. Novel 3′,5′- and 5′,5′-pyrophosphorothiolate-linked dinucleoside cap analogues were thereby prepared.

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Eguaogie, O., Cooke, L. A., Martin, P. M. L., Ravalico, F., Conway, L. P., Hodgson, D. R. W., … Vyle, J. S. (2016). Synthesis of novel pyrophosphorothiolate-linked dinucleoside cap analogues in a ball mill. Organic and Biomolecular Chemistry, 14(4), 1201–1205. https://doi.org/10.1039/c5ob02061a

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