Oligonuclecotides bearing phosphoramidate internucleotide linkages can be prepared chemically by standard solid‐phase DNA synthesis. Thus, phosphoramidate internucleotide bonds can be placed at will into specific positions within a given DNA fragment. The backbone‐modified DNA fragments prepared in this way are susceptible to a specific chemical cleavage.
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Willi Bannwarth (1988) studied this question.
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