Abstract
Acid mediated variations of 13C-NMR chemical shifts and destruction kinetics of protected deoxyguanosine derivatives indicate a pronounced effect of the electronegativity of the protecting groups on their stability.
| Original language | English |
|---|---|
| Pages (from-to) | 707-711 |
| Number of pages | 5 |
| Journal | Nucleosides and Nucleotides |
| Volume | 7 |
| Issue number | 5-6 |
| DOIs | |
| State | Published - 1 Oct 1988 |
Fingerprint
Dive into the research topics of 'On the influence of the nature of 2-n-protecting ACYL groups on the stability of deoxyguanosine derivatives'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver