Nucleotides Part XL. Synthesis and Characterization of Modified 2′–5′ Adenylate Trimers–Potential Antiviral Agents
✍ Scribed by Helga Schirmeister; Wolfgang Pfleiderer
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- German
- Weight
- 1000 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
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 for 2′‐OH protection in neighbourhood to the 3′‐O‐tbds residue was compared during the synthesis of the target trimers. For other functional positions, the use of the 2‐(4‐nitrophenyl)ethyl (npe) and 2‐(4‐nitrophenyl)ethoxycarbonyl (npeoc) blocking groups were favoured.
📜 SIMILAR VOLUMES
Some new (2'-5')oligoadenylate trimers, i e . , 22-28, containing the antiviral nucleoside ribavirin ( = 1 -(P-Dribofuranosyl)-1H-l,2,4-triazole-3-carboxamide; 7) and the synthetic cytokine 6-(benzylamino)purine riboside (= N6-benzyladenosine; 1) in different positions of the trimer, have been synth
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 phosp