cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol

The stereochemistry and regiochemistry of the title compound, C(18)H(18)O(2), were determined by the X-ray analysis. There are two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene rings are 88.31 (4) and 86.27 (4)°. The cyclo­hexene rings are in half-cha...

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Detalles Bibliográficos
Autores principales: Lough, Alan J., Raheem, Mohammed-Abdul, Tam, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011258/
https://www.ncbi.nlm.nih.gov/pubmed/24860354
http://dx.doi.org/10.1107/S1600536814007739
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author Lough, Alan J.
Raheem, Mohammed-Abdul
Tam, William
author_facet Lough, Alan J.
Raheem, Mohammed-Abdul
Tam, William
author_sort Lough, Alan J.
collection PubMed
description The stereochemistry and regiochemistry of the title compound, C(18)H(18)O(2), were determined by the X-ray analysis. There are two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene rings are 88.31 (4) and 86.27 (4)°. The cyclo­hexene rings are in half-chair conformations. In the crystal, O—H⋯O hydrogen bonds link alternating types of mol­ecules into chains along [010] with graph-set C (2) (2)(4).
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spelling pubmed-40112582014-05-23 cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol Lough, Alan J. Raheem, Mohammed-Abdul Tam, William Acta Crystallogr Sect E Struct Rep Online Organic Papers The stereochemistry and regiochemistry of the title compound, C(18)H(18)O(2), were determined by the X-ray analysis. There are two independent mol­ecules in the asymmetric unit in which the dihedral angles between the benzene rings are 88.31 (4) and 86.27 (4)°. The cyclo­hexene rings are in half-chair conformations. In the crystal, O—H⋯O hydrogen bonds link alternating types of mol­ecules into chains along [010] with graph-set C (2) (2)(4). International Union of Crystallography 2014-04-12 /pmc/articles/PMC4011258/ /pubmed/24860354 http://dx.doi.org/10.1107/S1600536814007739 Text en © Lough et al. 2014 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
Lough, Alan J.
Raheem, Mohammed-Abdul
Tam, William
cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title_full cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title_fullStr cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title_full_unstemmed cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title_short cis-2-(4-Meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
title_sort cis-2-(4-meth­oxy­phen­yl)-4-methyl-1,2-di­hydro­naphthalen-1-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011258/
https://www.ncbi.nlm.nih.gov/pubmed/24860354
http://dx.doi.org/10.1107/S1600536814007739
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