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. 1989 Aug 11;17(15):6129–6141. doi: 10.1093/nar/17.15.6129

Uncharged stereoregular nucleic acid analogs: 2. Morpholino nucleoside oligomers with carbamate internucleoside linkages.

E P Stirchak 1, J E Summerton 1, D D Weller 1
PMCID: PMC318266  PMID: 2771642

Abstract

A novel oligonucleotide analog has been prepared from ribonucleoside derived morpholine subunits linked by carbamate groups. Oxidative cleavage of the 2',3' vicinal diol of cytidine followed by reductive amination of the resulting dialdehyde afforded the morpholine subunit. Coupling of the subunits are through carbamate moieties and the oligomers were characterized by 1H NMR and FAB MS. Evidence for interaction of the hexamer 19 with p(dG6) was found, but an atypical interaction of 19 with a RNA target was observed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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