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MDPI, Molecules, 8(15), p. 5692-5707, 2010

DOI: 10.3390/molecules15085692

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Solid-Phase Synthesis of Oligodeoxynucleotides Containing N4-[2-(t-butyldisulfanyl)ethyl]-5-methylcytosine Moieties

Journal article published in 2010 by Sónia Pérez-Rentero, Alejandra V. Garibotti, Ramón Eritja ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

An efficient route for the synthesis of the phosphoramidite derivative of 5-methylcytosine bearing a tert-butylsulfanyl group protected thiol is described. This building block is used for the preparation of oligonucleotides carrying a thiol group at the nucleobase at the internal position of a DNA sequence. The resulting thiolated oligonucleotides are useful intermediates to generate oligonucleotide conjugates carrying molecules of interest at internal positions of a DNA sequence.