1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol

The title mol­ecule, C(18)H(24)O(12), has crystallographic 2/m symmetry with two acetate group located on a mirror plane. The H—Csp (3)—O—Csp (2) torsion angles characterizing orientation of the acetyl groups with respect to the cyclo­hexane ring are 0.0, 23.9 and −23.9°. The cyclo­hexane ring is in...

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Detalles Bibliográficos
Autores principales: Kant, Rajni, Gupta, Vivek K., Kapoor, Kamini, Chib, Renu, Shah, Bhahwal A., Taneja, Subhash C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415030/
https://www.ncbi.nlm.nih.gov/pubmed/22905017
http://dx.doi.org/10.1107/S1600536812033600
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author Kant, Rajni
Gupta, Vivek K.
Kapoor, Kamini
Chib, Renu
Shah, Bhahwal A.
Taneja, Subhash C.
author_facet Kant, Rajni
Gupta, Vivek K.
Kapoor, Kamini
Chib, Renu
Shah, Bhahwal A.
Taneja, Subhash C.
author_sort Kant, Rajni
collection PubMed
description The title mol­ecule, C(18)H(24)O(12), has crystallographic 2/m symmetry with two acetate group located on a mirror plane. The H—Csp (3)—O—Csp (2) torsion angles characterizing orientation of the acetyl groups with respect to the cyclo­hexane ring are 0.0, 23.9 and −23.9°. The cyclo­hexane ring is in a chair conformation with all substituents in equatorial positions. In the crystal, mol­ecules are connected through C—H⋯O hydrogen bonds into a chain extending along the c axis.
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spelling pubmed-34150302012-08-17 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol Kant, Rajni Gupta, Vivek K. Kapoor, Kamini Chib, Renu Shah, Bhahwal A. Taneja, Subhash C. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, C(18)H(24)O(12), has crystallographic 2/m symmetry with two acetate group located on a mirror plane. The H—Csp (3)—O—Csp (2) torsion angles characterizing orientation of the acetyl groups with respect to the cyclo­hexane ring are 0.0, 23.9 and −23.9°. The cyclo­hexane ring is in a chair conformation with all substituents in equatorial positions. In the crystal, mol­ecules are connected through C—H⋯O hydrogen bonds into a chain extending along the c axis. International Union of Crystallography 2012-07-28 /pmc/articles/PMC3415030/ /pubmed/22905017 http://dx.doi.org/10.1107/S1600536812033600 Text en © Kant et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Kant, Rajni
Gupta, Vivek K.
Kapoor, Kamini
Chib, Renu
Shah, Bhahwal A.
Taneja, Subhash C.
1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title_full 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title_fullStr 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title_full_unstemmed 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title_short 1,2,3,4,5,6-Hexa-O-acetyl-scyllo-inositol
title_sort 1,2,3,4,5,6-hexa-o-acetyl-scyllo-inositol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415030/
https://www.ncbi.nlm.nih.gov/pubmed/22905017
http://dx.doi.org/10.1107/S1600536812033600
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