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A part of this work appeared in a preliminary report: Imanishi T., Obika S. J. Synth. Org. Chem., Jpn. 57:1999;969.
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N3′-P5′ Phosphoramidate oligonucleotides are known to form a stable triplex with a homopurine·homopyrimidine tract in dsDNA. See:
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N3′-P5′ Phosphoramidate oligonucleotides are known to form a stable triplex with a homopurine·homopyrimidine tract in dsDNA. See: Gryaznov S.M., Chen J.-K. J. Am. Chem. Soc. 116:1994;3143.
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0030834244
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Only C-rich homopyrimidine sequences of peptide nucleic acids (PNA) can bind to dsDNA to form PNA·DNA·DNA triplex. See:
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Only C-rich homopyrimidine sequences of peptide nucleic acids (PNA) can bind to dsDNA to form PNA·DNA·DNA triplex. See: Wittung P., Nielsen P., Nordén B. Biochemistry. 36:1997;7973.
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0026341239
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However, except for the C-rich sequences, the strand invasion (PNA·DNA·PNA triplex formation) was favored. See:
-
However, except for the C-rich sequences, the strand invasion (PNA·DNA·PNA triplex formation) was favored. See: Nielsen P.E., Egholm M., Berg R.H., Buchardt O. Science. 254:1991;1497.
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Although the conformation of triplexes was believed to be A-form-like structures (N-form sugar puckering) from the X-ray fiber analysis of poly(dT)·poly(dA)·poly(dT), recent studies have shown that some triplex structures differ from the A form. See: New York: Springer-Verlag. pp 100-150
-
Although the conformation of triplexes was believed to be A-form-like structures (N-form sugar puckering) from the X-ray fiber analysis of poly(dT)·poly(dA)·poly(dT), recent studies have shown that some triplex structures differ from the A form. See: Soyfer V.N., Potaman V.N. Triple-Helical Nucleic Acids. 1996;Springer-Verlag, New York. pp 100-150.
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84987574125
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The stereochemistry of 5 was confirmed by the observation of NOE between the benzyliden hydrogen and 2′- or 3′-hydrogen. It is thought that the endo-isomer was selectively obtained thermodynamically. See:
-
The stereochemistry of 5 was confirmed by the observation of NOE between the benzyliden hydrogen and 2′- or 3′-hydrogen. It is thought that the endo-isomer was selectively obtained thermodynamically. See: Li C., Vasella A. Helv. Chim. Acta. 76:1993;211.
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