Abstract
Synthesis of 2′-deoxyguanosine tethered through N-2 to an imidazole is described. The modified 2′-deoxyguanosine was converted to two different phosphoramidites, one with and the other without a 6- O-protecting group. The phosphoramidites were incorporated into oligonucleotide alone or together with a 2′-deoxyuridine tethered to a bipyridine. Protection and deprotection of the imidazole are also briefly described.
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