Oligonucleotides derived from 5-(1-propynyl)-2′- O-allyl-uridine and 5-(1-propynyl)-2′- O-allyl-cytidine: Synthesis and RNA duplex formation

The protected nucleoside analogs of 5-(1-propynyl)-2′- O-allyl-uridine and 5-(1-propynyl)-2′- O-allyl-cytidine are described. Oligonucleotides containing this modification significantly enhance double-helix formation with single-strand RNA. The protected nucleoside analogs of 5-(1-propynyl)-2′- O-al...

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Published inTetrahedron letters Vol. 34; no. 6; pp. 1003 - 1006
Main Authors Froehler, Brian C., Jones, Robert J., Cao, Xiaodong, Terhorst, Terry J.
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 05.02.1993
Elsevier
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Summary:The protected nucleoside analogs of 5-(1-propynyl)-2′- O-allyl-uridine and 5-(1-propynyl)-2′- O-allyl-cytidine are described. Oligonucleotides containing this modification significantly enhance double-helix formation with single-strand RNA. The protected nucleoside analogs of 5-(1-propynyl)-2′- O-allyl-uridine and 5-(1-propynyl)-2′- O-allyl-cytidine are described. Oligonucleotides containing this modification significantly enhance double-helix formation with single-strand RNA.
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(00)77476-4