Stereospecific Synthesis of Aryl β-D-N-Acetylglucopyranosides by Phase Transfer Catalysis
Under phase transfer catalyzed conditions, 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl chloride (1) reacts with a series of phenoxides to afford high yields of acetylated aryl β-D-N-acetylgluco-pyranosides (3-8). Deprotection of the hydroxyl groups under Zemplén condition gave quantita...
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Veröffentlicht in: | Synthetic communications 1990-07, Vol.20 (14), p.2097-2102 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Under phase transfer catalyzed conditions, 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl chloride (1) reacts with a series of phenoxides to afford high yields of acetylated aryl β-D-N-acetylgluco-pyranosides (3-8). Deprotection of the hydroxyl groups under Zemplén condition gave quantitative yields of the free glycosides 3a-8a. |
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ISSN: | 0039-7911 1532-2432 |
DOI: | 10.1080/00397919008053144 |