n-Propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
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Published:2013-01-04
Issue:2
Volume:69
Page:o158-o158
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ISSN:1600-5368
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Container-title:Acta Crystallographica Section E Structure Reports Online
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language:
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Short-container-title:Acta Cryst E
Author:
Mönch Bettina,Emmerling Franziska,Kraus Werner,Becker Roland,Nehls Irene
Abstract
The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-propoxytetrahydro-2H-pyran-3,4,5-triyl triacetate], C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide andn-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant interactions such as hydrogen bonds.
Publisher
International Union of Crystallography (IUCr)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry