Über die Iodierung von Monosaccharid‐Derivaten mit Iodtrimethylsilan
Iodation of Monosaccharide Derivatives with Iodotrimethylsilane With iodotrimethylsilane generated in situ, iodine can be introduced into carbohydrate derivatives with high selectivity. The rate of iodination at the anomeric center of the C‐1‐substituted 2,3,4,6‐tetra‐O‐acetyl‐D‐glucopyranoses 1a–d...
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Veröffentlicht in: | Liebigs Annalen der Chemie 1984-05, Vol.1984 (5), p.1052-1055 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Iodation of Monosaccharide Derivatives with Iodotrimethylsilane
With iodotrimethylsilane generated in situ, iodine can be introduced into carbohydrate derivatives with high selectivity. The rate of iodination at the anomeric center of the C‐1‐substituted 2,3,4,6‐tetra‐O‐acetyl‐D‐glucopyranoses 1a–d decreases in the following series: OAc > OBz ≈ OH » OCH3. – Hydroxy groups or their ethers 3b, c react distinctively to give the trimethylsilyl ethers, whereas the primary react to yield the 6‐deoxy‐6‐iodo derivatives 5. The 1‐O‐acetyl‐6‐hydroxy derivative 6a and its 6‐O‐trityl ether form 2,3,4‐tri‐O‐acetyl‐6‐deoxy‐6‐iodo‐α‐D‐glucopyranosyl iodide (7). |
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ISSN: | 0170-2041 1099-0690 |
DOI: | 10.1002/jlac.198419840523 |