## Abstract The four protected diastereoisomcrs 7a/7b and 8a/8b __P__‐thioadenylyl‐(3′–5′)‐__P__‐thioadenylyI‐(3′–5′)‐adenosine were synthesized, separated, and deblocked to the free oligonucleotides (__Scheme__). Biochemical characterization of these (3′–5′)phosphorothioate analogues of adenyiate
Nucleotides. Part XXXVIII.. Syntheses and characterization of phosphorothioate analogues of (2′–5′) adenylate dimer and trimer and their 5′-O-monophosphates
✍ Scribed by Ramamurthy Charubala; Wolfgang Pfleiderer
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- German
- Weight
- 551 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Dedicated to Prof. Dr. Wilhelm Fleischhacker on the occasion of his 60th birthday (8.X1.91) ~ ~~
The chemical syntheses of the phosphorothioate of (2'-5')adenylate dimer (see 6a, 6b) and trimer (see 1 la, 1 lb, 12a, 12b) as well as of their 5'-monophosphates (see 15a, 15b, 16a, 16b) using the phosphoramidite method are described. The resulting diastereoisomer mixtures were separated into the pure components by chromatographical means. All synthetic intermediates were characterized by TLC, elemental analysis, and UV and 'H-NMR spectra.
📜 SIMILAR VOLUMES
## Abstract 2′–5′ Adenylate trimers 41–44 carrying the (__tert__‐butyl)dimethylsilyl (tbds) group at the 3′‐OH position of various sugar moieties were synthesized __via__ the phosphoramidite method. The use of the (__tert__‐butyloxy)carbonyl (boc) and 2‐(4‐nitrophenyl)ethylsulfonyl (npes) groups fo
Part XXVII [I].