**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 ac
Un nouvel analogue synthétique de l'adénosine: La désoxy-3′-C-dibromométhylidène-3′-adénosine
✍ Scribed by Jean M. J. Tronchet; Dominique Schwarzenbach
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 356 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
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‐configuration of the nucleoside was established by formation of a cyclonucleoside. 7 is very slowly deaminated by adenosine deaminase. In contrast with its dichloro analog, it does not inhibit the growth of Escherichia coli.
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