4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid

The racemic title compound, C(16)H(20)O(3), was synthesized to study the hydrogen-bonding inter­action of the two enanti­o­mers in the solid state. In the crystal structure, R and S pairs of the racemate are linked by pairs of inter­molecular O—H⋯O hydrogen bonds, producing centrosymmetric R (2) (2)...

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Detalles Bibliográficos
Autores principales: Xie, Songwen, Nusbaum, Dannette A., Stein, Holly J., Pink, Maren
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979377/
https://www.ncbi.nlm.nih.gov/pubmed/21579516
http://dx.doi.org/10.1107/S1600536810018544
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author Xie, Songwen
Nusbaum, Dannette A.
Stein, Holly J.
Pink, Maren
author_facet Xie, Songwen
Nusbaum, Dannette A.
Stein, Holly J.
Pink, Maren
author_sort Xie, Songwen
collection PubMed
description The racemic title compound, C(16)H(20)O(3), was synthesized to study the hydrogen-bonding inter­action of the two enanti­o­mers in the solid state. In the crystal structure, R and S pairs of the racemate are linked by pairs of inter­molecular O—H⋯O hydrogen bonds, producing centrosymmetric R (2) (2)(8) rings.
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spelling pubmed-29793772010-12-30 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid Xie, Songwen Nusbaum, Dannette A. Stein, Holly J. Pink, Maren Acta Crystallogr Sect E Struct Rep Online Organic Papers The racemic title compound, C(16)H(20)O(3), was synthesized to study the hydrogen-bonding inter­action of the two enanti­o­mers in the solid state. In the crystal structure, R and S pairs of the racemate are linked by pairs of inter­molecular O—H⋯O hydrogen bonds, producing centrosymmetric R (2) (2)(8) rings. International Union of Crystallography 2010-05-26 /pmc/articles/PMC2979377/ /pubmed/21579516 http://dx.doi.org/10.1107/S1600536810018544 Text en © Xie et al. 2010 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
Xie, Songwen
Nusbaum, Dannette A.
Stein, Holly J.
Pink, Maren
4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title_full 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title_fullStr 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title_full_unstemmed 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title_short 4-(3-Methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
title_sort 4-(3-methoxy­phen­yl)-2,6-dimethyl­cyclo­hex-3-enecarboxylic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979377/
https://www.ncbi.nlm.nih.gov/pubmed/21579516
http://dx.doi.org/10.1107/S1600536810018544
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AT nusbaumdannettea 43methoxyphenyl26dimethylcyclohex3enecarboxylicacid
AT steinhollyj 43methoxyphenyl26dimethylcyclohex3enecarboxylicacid
AT pinkmaren 43methoxyphenyl26dimethylcyclohex3enecarboxylicacid

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