(R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl

The asymmetric unit of the title compound, C(24)H(22)O(4), contains two independent mol­ecules in both of which the naphthalene ring systems adopts a transoid arrangement. The dihedral angles between the naphthalene ring system in the two mol­ecules are 83.0 (1) and 89.0 (1)°. There are slight diffe...

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Detalles Bibliográficos
Autores principales: Zhou, Liang, Eli, Wumanjiang
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/PMC3344493/
https://www.ncbi.nlm.nih.gov/pubmed/22590255
http://dx.doi.org/10.1107/S1600536812014699
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author Zhou, Liang
Eli, Wumanjiang
author_facet Zhou, Liang
Eli, Wumanjiang
author_sort Zhou, Liang
collection PubMed
description The asymmetric unit of the title compound, C(24)H(22)O(4), contains two independent mol­ecules in both of which the naphthalene ring systems adopts a transoid arrangement. The dihedral angles between the naphthalene ring system in the two mol­ecules are 83.0 (1) and 89.0 (1)°. There are slight differences in the C(H(3))—O—C(H(2))—O– torsion angles of the eqivalent meth­oxy­meth­oxy groups. In the crystal, weak C—H⋯O hydrogen bonds are present.
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spelling pubmed-33444932012-05-15 (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl Zhou, Liang Eli, Wumanjiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(24)H(22)O(4), contains two independent mol­ecules in both of which the naphthalene ring systems adopts a transoid arrangement. The dihedral angles between the naphthalene ring system in the two mol­ecules are 83.0 (1) and 89.0 (1)°. There are slight differences in the C(H(3))—O—C(H(2))—O– torsion angles of the eqivalent meth­oxy­meth­oxy groups. In the crystal, weak C—H⋯O hydrogen bonds are present. International Union of Crystallography 2012-04-13 /pmc/articles/PMC3344493/ /pubmed/22590255 http://dx.doi.org/10.1107/S1600536812014699 Text en © Zhou and Eli 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
Zhou, Liang
Eli, Wumanjiang
(R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title_full (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title_fullStr (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title_full_unstemmed (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title_short (R)-2,2′-Bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
title_sort (r)-2,2′-bis(meth­oxy­meth­oxy)-1,1′-binaphth­yl
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344493/
https://www.ncbi.nlm.nih.gov/pubmed/22590255
http://dx.doi.org/10.1107/S1600536812014699
work_keys_str_mv AT zhouliang r22bismethoxymethoxy11binaphthyl
AT eliwumanjiang r22bismethoxymethoxy11binaphthyl

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