Synthesis of 6-chloro-9-(6′-deoxy-3′-C-methyl-2′,3′,4′-tri-O-methyl- β-D-allopyranosyl)purine: a branched-chain sugar nucleoside
The preparation of 6-deoxy-3-C-methyl-2,3,4-tri-O-metliyl- D -allopyranose (7), a branclied-chain sugar with the same constitution as nogalose from the antibiotic nogalamycin, is described. Condensation of the 1-O-acetyl derivative 8 with 6-chloropurine by the fusion method gave 6-chloro-9-(6′-deoxy...
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Veröffentlicht in: | Canadian journal of chemistry 1968-12, Vol.46 (23), p.3691-3694 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The preparation of 6-deoxy-3-C-methyl-2,3,4-tri-O-metliyl-
D
-allopyranose (7), a branclied-chain sugar with the same constitution as nogalose from the antibiotic nogalamycin, is described. Condensation of the 1-O-acetyl derivative
8
with 6-chloropurine by the fusion method gave 6-chloro-9-(6′-deoxy-3′-C-methyl-2′,3′,4′-tri-O-methyl-β-
D
-allopyranosyl)purine (
9
), which to our knowledge is the first synthetic, purine nucleoside containing a branched-chain sugar with a pyranose ring. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v68-610 |