(2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one

In the title compound, C(21)H(23)NO(3), the central oxazolidinone ring is approximately planar, the maximum deviation from the plane through the central ring being 0.043 (1) Å. The tert-butyl and benzyl substituents are cis to each other and trans to the N-benzoyl group. The inter­planar angle betwe...

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Detalles Bibliográficos
Autores principales: Dungan, Victoria J., Mueller-Bunz, Helge, Rutledge, Peter J.
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/PMC3435759/
https://www.ncbi.nlm.nih.gov/pubmed/22969630
http://dx.doi.org/10.1107/S1600536812035556
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author Dungan, Victoria J.
Mueller-Bunz, Helge
Rutledge, Peter J.
author_facet Dungan, Victoria J.
Mueller-Bunz, Helge
Rutledge, Peter J.
author_sort Dungan, Victoria J.
collection PubMed
description In the title compound, C(21)H(23)NO(3), the central oxazolidinone ring is approximately planar, the maximum deviation from the plane through the central ring being 0.043 (1) Å. The tert-butyl and benzyl substituents are cis to each other and trans to the N-benzoyl group. The inter­planar angle between the aromatic rings of the C-benzyl and N-benzoyl groups is 81.10 (4)°.
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spelling pubmed-34357592012-09-11 (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one Dungan, Victoria J. Mueller-Bunz, Helge Rutledge, Peter J. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(23)NO(3), the central oxazolidinone ring is approximately planar, the maximum deviation from the plane through the central ring being 0.043 (1) Å. The tert-butyl and benzyl substituents are cis to each other and trans to the N-benzoyl group. The inter­planar angle between the aromatic rings of the C-benzyl and N-benzoyl groups is 81.10 (4)°. International Union of Crystallography 2012-08-23 /pmc/articles/PMC3435759/ /pubmed/22969630 http://dx.doi.org/10.1107/S1600536812035556 Text en © Dungan 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
Dungan, Victoria J.
Mueller-Bunz, Helge
Rutledge, Peter J.
(2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title_full (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title_fullStr (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title_full_unstemmed (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title_short (2S,4S)-3-Benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
title_sort (2s,4s)-3-benzoyl-4-benzyl-2-tert-but­yl-1,3-oxazolidin-5-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435759/
https://www.ncbi.nlm.nih.gov/pubmed/22969630
http://dx.doi.org/10.1107/S1600536812035556
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