Abstract
A new multifunctional dinucleotide analog is synthesized for the application in in vitro selection experiments with linker-coupled reactants. For this purpose it contains a 5′-pCC ligation site, three flexible hexaethylene glycol spacers, a photocleavable o-nitrobenzyl unit and a 3′-terminal carboxy-function which can be derivatized with potential reactants as demonstrated with three model compounds.
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