Cyclic oligodeoxyribonucleotides have been synthesized in satisfactory yields by an easy procedure using polyethylene glycol (PEG) as soluble supporting polymer. The present method is particularly suitable for a medium to large scale synthesis. Early studies involving biological properties of synthetic and natural cyclic oligonucleotides stimulated a great deal of interest in such kind of molecules. The recent findings that circular single-stranded oligodeoxyribonucleotides having two runs of pyrimidines can bind tightly and sequence selectively to single-stranded polypurine DNA and RNA by forming triple helical complexes open up new perspectives to the design of more efficient DNA- and RNA-binding molecules. Our attention is being focused on the synthesis of medium-sized rings, since none of the synthetic procedures described so far proved to be really suitable for the preparation of such molecules on a relatively large scale. Following “classical” solution methods, which in principle should easily allow syntheses. © 1993, Taylor & Francis Group, LLC. All rights reserved.

Peg-Supported synthesis of cyclic oligodeoxyribonucleotides

MESSERE, Anna;
1993

Abstract

Cyclic oligodeoxyribonucleotides have been synthesized in satisfactory yields by an easy procedure using polyethylene glycol (PEG) as soluble supporting polymer. The present method is particularly suitable for a medium to large scale synthesis. Early studies involving biological properties of synthetic and natural cyclic oligonucleotides stimulated a great deal of interest in such kind of molecules. The recent findings that circular single-stranded oligodeoxyribonucleotides having two runs of pyrimidines can bind tightly and sequence selectively to single-stranded polypurine DNA and RNA by forming triple helical complexes open up new perspectives to the design of more efficient DNA- and RNA-binding molecules. Our attention is being focused on the synthesis of medium-sized rings, since none of the synthetic procedures described so far proved to be really suitable for the preparation of such molecules on a relatively large scale. Following “classical” solution methods, which in principle should easily allow syntheses. © 1993, Taylor & Francis Group, LLC. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11591/193982
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