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(4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate
In the crystal structure of the title compound, C(14)H(17)NO(4), obtained by the reaction of N-benzoxycarbonyl-l-valine, paraformaldehyde and 4-methylbenzenesulfonic acid, molecules are linked by C—H⋯O hydrogen bonds, generating linear chains parallel to the a axis. C—H⋯π interactions of stacked...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961013/ https://www.ncbi.nlm.nih.gov/pubmed/21202077 http://dx.doi.org/10.1107/S1600536808004455 |
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author | Wu, Jian-Bin Lin, Kan Guo, Jian-Nan Tang, Guo Zhao, Yu-Fen |
author_facet | Wu, Jian-Bin Lin, Kan Guo, Jian-Nan Tang, Guo Zhao, Yu-Fen |
author_sort | Wu, Jian-Bin |
collection | PubMed |
description | In the crystal structure of the title compound, C(14)H(17)NO(4), obtained by the reaction of N-benzoxycarbonyl-l-valine, paraformaldehyde and 4-methylbenzenesulfonic acid, molecules are linked by C—H⋯O hydrogen bonds, generating linear chains parallel to the a axis. C—H⋯π interactions of stacked benzene rings also provide stability for the crystal structure. |
format | Text |
id | pubmed-2961013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29610132010-12-30 (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate Wu, Jian-Bin Lin, Kan Guo, Jian-Nan Tang, Guo Zhao, Yu-Fen Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(14)H(17)NO(4), obtained by the reaction of N-benzoxycarbonyl-l-valine, paraformaldehyde and 4-methylbenzenesulfonic acid, molecules are linked by C—H⋯O hydrogen bonds, generating linear chains parallel to the a axis. C—H⋯π interactions of stacked benzene rings also provide stability for the crystal structure. International Union of Crystallography 2008-03-12 /pmc/articles/PMC2961013/ /pubmed/21202077 http://dx.doi.org/10.1107/S1600536808004455 Text en © Wu et al. 2008 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 Wu, Jian-Bin Lin, Kan Guo, Jian-Nan Tang, Guo Zhao, Yu-Fen (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title | (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title_full | (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title_fullStr | (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title_full_unstemmed | (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title_short | (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
title_sort | (4s)-benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961013/ https://www.ncbi.nlm.nih.gov/pubmed/21202077 http://dx.doi.org/10.1107/S1600536808004455 |
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