1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate

The title compound, C(24)H(26)N(2)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopts a chair conformation. The two pyridine rings form a dihedral angle of 41.02 (4)°. In the crystal, mol­ecules are linked via C—H⋯O and C—H⋯N hydrogen bonds into a layer parallel...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Lim, Ming Yeng, Quah, Ching Kheng, Wu, Dongdong
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/PMC3379234/
https://www.ncbi.nlm.nih.gov/pubmed/22719432
http://dx.doi.org/10.1107/S1600536812018508
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author Fun, Hoong-Kun
Lim, Ming Yeng
Quah, Ching Kheng
Wu, Dongdong
author_facet Fun, Hoong-Kun
Lim, Ming Yeng
Quah, Ching Kheng
Wu, Dongdong
author_sort Fun, Hoong-Kun
collection PubMed
description The title compound, C(24)H(26)N(2)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopts a chair conformation. The two pyridine rings form a dihedral angle of 41.02 (4)°. In the crystal, mol­ecules are linked via C—H⋯O and C—H⋯N hydrogen bonds into a layer parallel to the bc plane.
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spelling pubmed-33792342012-06-20 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate Fun, Hoong-Kun Lim, Ming Yeng Quah, Ching Kheng Wu, Dongdong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(26)N(2)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopts a chair conformation. The two pyridine rings form a dihedral angle of 41.02 (4)°. In the crystal, mol­ecules are linked via C—H⋯O and C—H⋯N hydrogen bonds into a layer parallel to the bc plane. International Union of Crystallography 2012-05-05 /pmc/articles/PMC3379234/ /pubmed/22719432 http://dx.doi.org/10.1107/S1600536812018508 Text en © Fun 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
Fun, Hoong-Kun
Lim, Ming Yeng
Quah, Ching Kheng
Wu, Dongdong
1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title_full 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title_fullStr 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title_full_unstemmed 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title_short 1,1′-Bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
title_sort 1,1′-bicyclo­hexyl-1,1′-diyl 2,2′-bipyridine-3,3′-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379234/
https://www.ncbi.nlm.nih.gov/pubmed/22719432
http://dx.doi.org/10.1107/S1600536812018508
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AT quahchingkheng 11bicyclohexyl11diyl22bipyridine33dicarboxylate
AT wudongdong 11bicyclohexyl11diyl22bipyridine33dicarboxylate

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