N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)

In the title compound, C(20)H(26)N(2)O(4)S(2), the cyclo­hexane ring has a chair conformation. The two chiral C atoms are in S configurations. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [001]. Weak inter­molecular C—H⋯O hydrogen bonds further...

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Detalles Bibliográficos
Autores principales: Hong, Yi-Ling, Tan, Hua-Jie, Shen, Liang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089204/
https://www.ncbi.nlm.nih.gov/pubmed/21754435
http://dx.doi.org/10.1107/S1600536811012372
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author Hong, Yi-Ling
Tan, Hua-Jie
Shen, Liang
author_facet Hong, Yi-Ling
Tan, Hua-Jie
Shen, Liang
author_sort Hong, Yi-Ling
collection PubMed
description In the title compound, C(20)H(26)N(2)O(4)S(2), the cyclo­hexane ring has a chair conformation. The two chiral C atoms are in S configurations. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [001]. Weak inter­molecular C—H⋯O hydrogen bonds further stabilize the crystal packing.
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spelling pubmed-30892042011-07-13 N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide) Hong, Yi-Ling Tan, Hua-Jie Shen, Liang Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(26)N(2)O(4)S(2), the cyclo­hexane ring has a chair conformation. The two chiral C atoms are in S configurations. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [001]. Weak inter­molecular C—H⋯O hydrogen bonds further stabilize the crystal packing. International Union of Crystallography 2011-04-13 /pmc/articles/PMC3089204/ /pubmed/21754435 http://dx.doi.org/10.1107/S1600536811012372 Text en © Hong et al. 2011 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
Hong, Yi-Ling
Tan, Hua-Jie
Shen, Liang
N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title_full N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title_fullStr N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title_full_unstemmed N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title_short N,N′-[(1S,2S)-Cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
title_sort n,n′-[(1s,2s)-cyclo­hexane-1,2-di­yl]bis­(4-methyl­benzene­sulfonamide)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089204/
https://www.ncbi.nlm.nih.gov/pubmed/21754435
http://dx.doi.org/10.1107/S1600536811012372
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AT tanhuajie nn1s2scyclohexane12diylbis4methylbenzenesulfonamide
AT shenliang nn1s2scyclohexane12diylbis4methylbenzenesulfonamide

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