**A novel synthetic analog of adenosine: the 3′‐deoxy‐3′‐__C__‐dibromomenthylidene‐adenosine** The title compound (**7**) has been prepared by a sequence of classical synthetic steps from 3‐deoxy‐3‐__C__‐dibromomethylidene‐1,2: 5,6‐di‐__O__‐isopropylidene‐α‐D‐__ribo__‐hexofuranose (**1**). The β‐co
Un nouvel exemple de nucléoside à sucre ramifié insaturé: la désoxy-3′-méthylidène-3′-adénosine
✍ Scribed by Jean M. J. Tronchet; Jeannine F. Tronchet
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- German
- Weight
- 303 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
A Novel Example of Unsaturated Branched‐chain Sugar Nucleoside: 3′‐Deoxy‐3′‐methylidene‐adenosine
Starting from 5‐O‐benzoyl‐3‐C‐methylidene‐3‐deoxy‐1,2‐O‐isopropylidene‐α‐D‐erythro‐pentofuranose (11) the title compound 8 has been prepared. Its α‐anomer (9) and the acyclic sugar nucleoside 10 have been obtained as by‐products. Adenosine deaminase slowly deaminated 8, 9 being not affected. Compound 8 exhibited no antiviral activity, whereas one of its saturated analogues (13) inhibited the multiplication of the herpes‐1 (HF) virus.
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**Electron Impact Mass Spectrometry of the 3‐Desoxy‐1,2: 5,6‐di‐__O__‐isopropylidene‐3‐methylidene‐δ‐D‐hexofuranose and Some C(3′)‐Substituted Analogues** The mass spectra of the 3‐desoxy‐1,2:5, 6‐di‐__O__‐isopropylidene‐3‐methylidene‐ α‐D‐__ribo__‐hexofuranose and of some C(3′)‐mono‐ and ‐disubsti