## Abstract Treated with 2,3‐dimethyl‐2,3‐bis‐(hydroxylamino)‐butane, aldehydo‐dialdofuranoses (**1**) gave a mixture of two compounds: a 1,3‐dihydroxyimidazolidine (**2**) and a 1‐hydroxyimidazoline (**3**). Oxidation (PbO~2~) of compounds **3** gave stable free radicals having the structure of 2‐
Nouveaux exemples de radicaux libres stables de dérivés hétérocycliques de sucres. Communication préliminaire
✍ Scribed by Jean M. J. Tronchet; Joëlle Ojha-Poncet; Eva Winter-Mihaly; Boris Kohler; Michel Geoffroy
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 214 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Some more examples of stable free radicals of carbohydrate heterocyclic derivatives
2‐Glycosyl‐4,4,5,5‐tetramethylimidazoline‐ 3‐oxide‐1‐oxyls and 2‐glycosyl‐4,4,5,5‐tetramethylimidazoline 1‐oxyls have been prepared in nine carbohydrate series, which proves the generality of the method. The hyperfine coupling constant between the free electron and the α‐proton of the glycosyl group is never very large (0‐2.3 G) but a correlation between its value and the structure of the aglycone has been noted. Free radicals of that type, stable in aqueous solutions, are potentially interesting for biological studies.
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