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

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

The title compound, C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and propan-2-ol. The central ring adopts a chair conformation. The crystal does not contain any significant intermolecular interactions.

Bibliographic Details
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?S1600536812051483
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spelling doaj-700728671c854deabb91935c4ec008f52020-11-24T21:30:48ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-02-01692o157o15710.1107/S1600536812051483Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosideBettina MönchFranziska EmmerlingWerner KrausRoland BeckerIrene NehlsThe title compound, C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and propan-2-ol. The central ring adopts a chair conformation. The crystal does not contain any significant intermolecular interactions.http://scripts.iucr.org/cgi-bin/paper?S1600536812051483
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
Isopropyl 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 Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_short Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_full Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_fullStr Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_full_unstemmed Isopropyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyranoside
title_sort isopropyl 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, C17H26O10, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and propan-2-ol. The central ring adopts a chair conformation. The crystal does not contain any significant intermolecular interactions.
url http://scripts.iucr.org/cgi-bin/paper?S1600536812051483
work_keys_str_mv AT bettinam246nch isopropyl2346tetraoacetyl946dglucopyranoside
AT franziskaemmerling isopropyl2346tetraoacetyl946dglucopyranoside
AT wernerkraus isopropyl2346tetraoacetyl946dglucopyranoside
AT rolandbecker isopropyl2346tetraoacetyl946dglucopyranoside
AT irenenehls isopropyl2346tetraoacetyl946dglucopyranoside
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