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
Hauptverfasser: Howarth, G. B, Szarek, W. A, Jones, J. K. N
Format: Artikel
Sprache:eng
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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.
ISSN:0008-4042
1480-3291
DOI:10.1139/v68-610