4.4 Article

Thioctic acid modification of oligonucleotides using an H-phosphonate

Journal

TETRAHEDRON LETTERS
Volume 51, Issue 44, Pages 5787-5790

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.08.107

Keywords

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Funding

  1. EPSRC

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The H-phosphonate of a derivative of thioctic acid (TA) was synthesised and used to introduce a disulfide moiety at the 5'-end of oligonucleotides. This method overcomes the difficulties experienced with the phosphoramidite approach when employing a cyclic disulfide in the starting alcohol. The disulfide-modified oligonucleotides are subsequently used in metallic nanoparticle (Au and Ag) and surface functionalisation for sensitive, sequence specific analytical detection strategies. (C) 2010 Elsevier Ltd. All rights reserved.

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