Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate

In the title compound, C(18)H(19)NO(5)S, the five-membered isoxazolidine ring is in a half-chair conformation, and the phenyl rings are oriented at a dihedral angle of 66.53 (3)°. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional supra­molecular structure. A weak C—H⋯...

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Autores principales: Gültekin, Zeynep, Civan, Mehmet, Frey, Wolfgang, Hökelek, Tuncer
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/PMC4051012/
https://www.ncbi.nlm.nih.gov/pubmed/24940296
http://dx.doi.org/10.1107/S1600536814012161
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author Gültekin, Zeynep
Civan, Mehmet
Frey, Wolfgang
Hökelek, Tuncer
author_facet Gültekin, Zeynep
Civan, Mehmet
Frey, Wolfgang
Hökelek, Tuncer
author_sort Gültekin, Zeynep
collection PubMed
description In the title compound, C(18)H(19)NO(5)S, the five-membered isoxazolidine ring is in a half-chair conformation, and the phenyl rings are oriented at a dihedral angle of 66.53 (3)°. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional supra­molecular structure. A weak C—H⋯π inter­action is also observed between adjacent mol­ecules.
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spelling pubmed-40510122014-06-17 Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate Gültekin, Zeynep Civan, Mehmet Frey, Wolfgang Hökelek, Tuncer Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(19)NO(5)S, the five-membered isoxazolidine ring is in a half-chair conformation, and the phenyl rings are oriented at a dihedral angle of 66.53 (3)°. In the crystal, C—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional supra­molecular structure. A weak C—H⋯π inter­action is also observed between adjacent mol­ecules. International Union of Crystallography 2014-05-31 /pmc/articles/PMC4051012/ /pubmed/24940296 http://dx.doi.org/10.1107/S1600536814012161 Text en © Gültekin 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
Gültekin, Zeynep
Civan, Mehmet
Frey, Wolfgang
Hökelek, Tuncer
Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title_full Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title_fullStr Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title_full_unstemmed Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title_short Methyl 2-[(3RS,4RS)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
title_sort methyl 2-[(3rs,4rs)-3-phenyl-4-(phenyl­sulfon­yl)isoxazolidin-2-yl]acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051012/
https://www.ncbi.nlm.nih.gov/pubmed/24940296
http://dx.doi.org/10.1107/S1600536814012161
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AT hokelektuncer methyl23rs4rs3phenyl4phenylsulfonylisoxazolidin2ylacetate

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