(2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid

In the title racemic compound, C(11)H(16)O(3), the mol­ecule adopts a conformation that places its carboxyl group in an equatorial position. Mol­ecules aggregate by hydrogen-bond pairing of carboxyl groups, yielding centrosymmetric dimers that are arranged into layers in the (020) planes.

Detalles Bibliográficos
Autores principales: Efthimiopoulos, Georgia, Davison, Mark, Lalancette, Roger A., Thompson, Hugh W.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968079/
https://www.ncbi.nlm.nih.gov/pubmed/21581624
http://dx.doi.org/10.1107/S1600536808042700
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author Efthimiopoulos, Georgia
Davison, Mark
Lalancette, Roger A.
Thompson, Hugh W.
author_facet Efthimiopoulos, Georgia
Davison, Mark
Lalancette, Roger A.
Thompson, Hugh W.
author_sort Efthimiopoulos, Georgia
collection PubMed
description In the title racemic compound, C(11)H(16)O(3), the mol­ecule adopts a conformation that places its carboxyl group in an equatorial position. Mol­ecules aggregate by hydrogen-bond pairing of carboxyl groups, yielding centrosymmetric dimers that are arranged into layers in the (020) planes.
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spelling pubmed-29680792010-12-30 (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid Efthimiopoulos, Georgia Davison, Mark Lalancette, Roger A. Thompson, Hugh W. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title racemic compound, C(11)H(16)O(3), the mol­ecule adopts a conformation that places its carboxyl group in an equatorial position. Mol­ecules aggregate by hydrogen-bond pairing of carboxyl groups, yielding centrosymmetric dimers that are arranged into layers in the (020) planes. International Union of Crystallography 2008-12-20 /pmc/articles/PMC2968079/ /pubmed/21581624 http://dx.doi.org/10.1107/S1600536808042700 Text en © Efthimiopoulos et al. 2009 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
Efthimiopoulos, Georgia
Davison, Mark
Lalancette, Roger A.
Thompson, Hugh W.
(2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title_full (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title_fullStr (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title_full_unstemmed (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title_short (2SR,4aSR,8aSR)-6-Oxoperhydro­naphthalene-2-carboxylic acid
title_sort (2sr,4asr,8asr)-6-oxoperhydro­naphthalene-2-carboxylic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968079/
https://www.ncbi.nlm.nih.gov/pubmed/21581624
http://dx.doi.org/10.1107/S1600536808042700
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AT lalancetterogera 2sr4asr8asr6oxoperhydronaphthalene2carboxylicacid
AT thompsonhughw 2sr4asr8asr6oxoperhydronaphthalene2carboxylicacid

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