**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
Amino-nucléosides IV (Amino-3-désoxy-3-érythrofurannosyl)-9-adénine
✍ Scribed by Jean M. J. Tronchet; René Graf
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 352 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The synthesis of 9‐(3‐amino‐3‐deoxy‐β‐L‐(and D)‐erythrofuranosyl)‐adenine is described. This compound is a close analog of the aminonucleoside of puromycin.
📜 SIMILAR VOLUMES
La rifirence [l] constitue la premiere communication dc cette sirie. Une communication plus d6taillie est destinee & paraftre dans cette revue.
**Synthesis and enzymatic deamination of 3′‐__C__‐hydroxymethyl‐ and 3′‐__C__‐methyl‐β‐D‐xylofuranosyl‐9‐adenines** The title compounds have been prepared by classical synthetic steps after having optimized the nature of the blocking groups. Both nucleosides were found to be substrates of adenosine