Abstract
Substituted 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues have been synthesised from 5-alkynyl-uridine derivatives, incorporated into triplex forming oligonucleotides (TFOs) and found to selectively bind CG inversions with enhanced affinity compared to T.
| Original language | English |
|---|---|
| Pages (from-to) | 2555-2557 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 28 May 2005 |
Keywords
- Base Pairing
- Cytosine/analysis
- DNA/chemistry
- Guanine/analysis
- Hydrogen Bonding
- Nucleic Acid Conformation
- Nucleosides/chemical synthesis
- Oligonucleotides/chemistry
- Pyrimidinones/chemical synthesis
- Thymine/analysis