Abstract
The synthesis of two anthraquinone phosphoramidites is described. In both cases the anthraquinone moiety is attached via a linker to the 5-position of a uracil base, allowing incorporation at any thymidine position in an oligonucleotide sequence. Anthraquinone-modified oligonucleotides have potential applications as triplex stabilizers and fluorescence quenchers.
Acknowledgments
This research is funded by BBSRC. All oligonucleotide synthesis and purification was carried out by ATDBio Ltd., UK (www.atdbio.com).