## 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.
Amino-nucléosides. V. Amino-3′-didésoxy-3′, 5′-adénosine
✍ Scribed by Jean M. J. Tronchet; René Graf; Jeannine Tronchet
- Book ID
- 102855507
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 654 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A synthesis of 3′‐amino‐3′, 5′‐dideoxyadenosine is described. This compound is not a substrate of adenosine deaminase.
📜 SIMILAR VOLUMES
## Abstract The 3‐amino‐3,5‐didesoxy‐1,2‐O‐isopropylidene‐α‐D‐ribofuranose and ‐β‐D‐lyxo‐furanose and several derivatives thereof have been prepared by hydride reduction of the corresponding oximes.
**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
La rifirence [l] constitue la premiere communication dc cette sirie. Une communication plus d6taillie est destinee & paraftre dans cette revue.