Oligonucleotide conjugates containing fluorescein residues in the sugar phosphate back bone were synthesized by the standard solid phase phosphoramidite method using phosphor amidites of 9 [2 deoxy 5 O (4,4´ dimethoxytrityl) 2 methoxalylamino β D ribofurano syl] and 9 [2 deoxy 5 O (4,4´ dimethoxytrityl) 2 methoxalylamino β D arabinofuranosyl] N 6 benzoyladenine. The relative efficiency of the oligonucleotide synthesis with modified phosphoramidites was estimated.
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