(R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate

The structure of the title compound, C(20)H(21)NO(6)S, is of inter­est with respect to its anti­bacterial properties. The oxazolidine ring makes dihedral angles of 79.63 (14) and 56.16 (12)° with the phenyl and benzene rings, respectively, while the phenyl and benzene rings make a dihedral angle of...

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Detalles Bibliográficos
Autores principales: Li, Feng, Zhao, Ming-Zhong, Jin, Chun-Hua, Zou, Jian-Wei
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/PMC4011233/
https://www.ncbi.nlm.nih.gov/pubmed/24860399
http://dx.doi.org/10.1107/S1600536814009106
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author Li, Feng
Zhao, Ming-Zhong
Jin, Chun-Hua
Zou, Jian-Wei
author_facet Li, Feng
Zhao, Ming-Zhong
Jin, Chun-Hua
Zou, Jian-Wei
author_sort Li, Feng
collection PubMed
description The structure of the title compound, C(20)H(21)NO(6)S, is of inter­est with respect to its anti­bacterial properties. The oxazolidine ring makes dihedral angles of 79.63 (14) and 56.16 (12)° with the phenyl and benzene rings, respectively, while the phenyl and benzene rings make a dihedral angle of 64.37 (13)°. In the crystal, non-classical C—H⋯O hydrogen bonds link adjacent mol­ecules along the c axis.
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spelling pubmed-40112332014-05-23 (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate Li, Feng Zhao, Ming-Zhong Jin, Chun-Hua Zou, Jian-Wei Acta Crystallogr Sect E Struct Rep Online Organic Papers The structure of the title compound, C(20)H(21)NO(6)S, is of inter­est with respect to its anti­bacterial properties. The oxazolidine ring makes dihedral angles of 79.63 (14) and 56.16 (12)° with the phenyl and benzene rings, respectively, while the phenyl and benzene rings make a dihedral angle of 64.37 (13)°. In the crystal, non-classical C—H⋯O hydrogen bonds link adjacent mol­ecules along the c axis. International Union of Crystallography 2014-04-26 /pmc/articles/PMC4011233/ /pubmed/24860399 http://dx.doi.org/10.1107/S1600536814009106 Text en © Li 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
Li, Feng
Zhao, Ming-Zhong
Jin, Chun-Hua
Zou, Jian-Wei
(R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title_full (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title_fullStr (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title_full_unstemmed (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title_short (R)-[(R)-3-Benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
title_sort (r)-[(r)-3-benzyl-2-oxooxazolidin-4-yl][4-(methyl­sulfon­yl)phen­yl]methyl acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011233/
https://www.ncbi.nlm.nih.gov/pubmed/24860399
http://dx.doi.org/10.1107/S1600536814009106
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