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1. Structures I and II represent the previously synthesized, most promising amide modifications. a) Lebreton, J.; Waldner, A.; Lesueur, C.; De Mesmaeker, A. Synlett 1994, 137-140.
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m of I. However, the oligonucleotides used contained only thymidine as a base
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For synthesis of oligonucleotides see ref. 14 in
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12. For synthesis of oligonucleotides see ref. 14 in: De Mesmaeker, A.; Lebreton, J.; Hoffmann, P.; Freier, S.M. Synlett 1993, 677-697.
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