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N-Propyl 2,3,4,6-tetra-O-acetyl-?-d-glucopyran-oside.

ABSTRACT: THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-2H-pyran-3,4,5-triyl triacetate], C(17)H(26)O(10), was formed by a Koenigs-Knorr reaction of 2,3,4,6-tetra-O-acetyl-?-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant inter-actions such as hydrogen bonds.

SUBMITTER: Monch B

PROVIDER: S-EPMC3569225 | biostudies-literature | 2013 Feb

REPOSITORIES: biostudies-literature

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n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran-oside.

Mönch Bettina B Emmerling Franziska F Kraus Werner W Becker Roland R Nehls Irene I

Acta crystallographica. Section E, Structure reports online 20130104 Pt 2

THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-2H-pyran-3,4,5-triyl triacetate], C(17)H(26)O(10), was formed by a Koenigs-Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant inter-actions such as hydrogen bonds. ...[more]

PMID: 23424448

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