n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside

n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside

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 and n-propanol. The central ring adopts a chair conf...

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Main Authors: Bettina Mönch, Franziska Emmerling, Werner Kraus, Roland Becker, Irene Nehls
Format: Article
Language:English
Published: International Union of Crystallography 2013-02-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536812051495
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spelling doaj-40fb9611b13c45718e88129d6caeddd62020-11-25T01:35:52ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-02-01692o158o15810.1107/S1600536812051495n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosideBettina MönchFranziska EmmerlingWerner KrausRoland BeckerIrene NehlsThe 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 and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant interactions such as hydrogen bonds.http://scripts.iucr.org/cgi-bin/paper?S1600536812051495
collection DOAJ
language English
format Article
sources DOAJ
author Bettina Mönch
Franziska Emmerling
Werner Kraus
Roland Becker
Irene Nehls
spellingShingle Bettina Mönch
Franziska Emmerling
Werner Kraus
Roland Becker
Irene Nehls
n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
Acta Crystallographica Section E
author_facet Bettina Mönch
Franziska Emmerling
Werner Kraus
Roland Becker
Irene Nehls
author_sort Bettina Mönch
title n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_short n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_full n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_fullStr n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_full_unstemmed n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_sort n-propyl 2,3,4,6-tetra-o-acetyl-β-d-glucopyranoside
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2013-02-01
description 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 and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant interactions such as hydrogen bonds.
url http://scripts.iucr.org/cgi-bin/paper?S1600536812051495
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AT franziskaemmerling npropyl2346tetraoacetyl946dglucopyranoside
AT wernerkraus npropyl2346tetraoacetyl946dglucopyranoside
AT rolandbecker npropyl2346tetraoacetyl946dglucopyranoside
AT irenenehls npropyl2346tetraoacetyl946dglucopyranoside
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