Ontology highlight
ABSTRACT:
SUBMITTER: Ng PS
PROVIDER: S-EPMC2933660 | biostudies-literature | 2010 Aug
REPOSITORIES: biostudies-literature
Ng Pei-Sze PS Laing Brian M BM Balasundarum Ganesan G Pingle Maneesh M Friedman Alan A Bergstrom Donald E DE
Bioconjugate chemistry 20100801 8
A series of aliphatic and aromatic spacer molecules designed to cap the ends of DNA duplexes have been synthesized. The spacers were converted into dimethoxytrityl-protected phosphoramidites as synthons for oligonucleotides synthesis. The effect of the spacers on the stability of short DNA duplexes was assessed by melting temperature studies. End-caps containing amide groups were found to be less stabilizing than the hexaethylene glycol spacer. End-caps containing either a terthiophene or a naph ...[more]