𝔖 Bobbio Scriptorium
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Amino-nucléosides III. Dérivés des amino-3-didésoxy-3,5-D-lyxo et D-ribo-pentoses

✍ Scribed by J. M. J. Tronchet; R. Graf

Book ID
102855343
Publisher
John Wiley and Sons
Year
1972
Tongue
German
Weight
647 KB
Volume
55
Category
Article
ISSN
0018-019X

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✦ Synopsis

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.

📜 SIMILAR VOLUMES

Amino-nucléosides IV (Amino-3-désoxy-3-é
Amino-nucléosides IV (Amino-3-désoxy-3-érythrofurannosyl)-9-adénine
✍ Jean M. J. Tronchet; René Graf 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 German ⚖ 352 KB

## 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.

Synthèse des 2-amino-2-désoxy-d-arabinon
Synthèse des 2-amino-2-désoxy-d-arabinono- et -d-xylono-lactones par condensation d'acides aminés avec le d-glycéraldéhyde. Analyse structurale par rayons X de deux dérivés
✍ Jean-Claude Depezay; Annie Dureault; Thierry Prange 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 626 KB

Synthesis of 2-amino-2-deoxy-D-pentonolactones was performed by diastereoselective hydroxyalkylation of 2,3-0-isopropylidene-D-glyceraldehyde with ethyl isocyanoacetate, to give two oxazolines in a ratio of 7:3. Hydrolysis gave first the corresponding amides, and then the 2-amino-2-deoxypentonolacto