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(4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine
The absolute configuration of the title compound, C(20)H(23)NO(2), has been confirmed as 4S. The benzyl residue and H atom at the asymmetric C-atom centre occupy pseudo-axial and bisectional positions, respectively. The oxazolidine ring adopts an envelope conformation. In the crystal structure, the...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009175/ https://www.ncbi.nlm.nih.gov/pubmed/21589035 http://dx.doi.org/10.1107/S1600536810040699 |
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author | Gzella, Andrzej K. Chrzanowska, Maria Dreas, Agnieszka Meissner, Zofia |
author_facet | Gzella, Andrzej K. Chrzanowska, Maria Dreas, Agnieszka Meissner, Zofia |
author_sort | Gzella, Andrzej K. |
collection | PubMed |
description | The absolute configuration of the title compound, C(20)H(23)NO(2), has been confirmed as 4S. The benzyl residue and H atom at the asymmetric C-atom centre occupy pseudo-axial and bisectional positions, respectively. The oxazolidine ring adopts an envelope conformation. In the crystal structure, the molecular packing is stabilized by non-classical C—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-3009175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30091752010-12-30 (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine Gzella, Andrzej K. Chrzanowska, Maria Dreas, Agnieszka Meissner, Zofia Acta Crystallogr Sect E Struct Rep Online Organic Papers The absolute configuration of the title compound, C(20)H(23)NO(2), has been confirmed as 4S. The benzyl residue and H atom at the asymmetric C-atom centre occupy pseudo-axial and bisectional positions, respectively. The oxazolidine ring adopts an envelope conformation. In the crystal structure, the molecular packing is stabilized by non-classical C—H⋯O hydrogen bonds. International Union of Crystallography 2010-10-20 /pmc/articles/PMC3009175/ /pubmed/21589035 http://dx.doi.org/10.1107/S1600536810040699 Text en © Gzella et al. 2010 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 Gzella, Andrzej K. Chrzanowska, Maria Dreas, Agnieszka Meissner, Zofia (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title | (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title_full | (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title_fullStr | (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title_full_unstemmed | (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title_short | (4S)-(−)-4-Benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
title_sort | (4s)-(−)-4-benzyl-2,2-dimethyl-3-o-toluoyl-1,3-oxazolidine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009175/ https://www.ncbi.nlm.nih.gov/pubmed/21589035 http://dx.doi.org/10.1107/S1600536810040699 |
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