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meso-3,6-Dioxopiperazine-2,5-diacetamide
The title compound, C(8)H(12)N(4)O(4), was obtained by cyclization of the two l-asparagine molecules and reveals a crystallographic inversion symmetry, and accordingly the two stereogenic centres are of opposite chirality. Thus, an asymmetric unit comprises a half of a molecule. The molecules are...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247435/ https://www.ncbi.nlm.nih.gov/pubmed/22220053 http://dx.doi.org/10.1107/S1600536811043376 |
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author | Li, Ping Zhang, Chun Xu, Wei |
author_facet | Li, Ping Zhang, Chun Xu, Wei |
author_sort | Li, Ping |
collection | PubMed |
description | The title compound, C(8)H(12)N(4)O(4), was obtained by cyclization of the two l-asparagine molecules and reveals a crystallographic inversion symmetry, and accordingly the two stereogenic centres are of opposite chirality. Thus, an asymmetric unit comprises a half of a molecule. The molecules are assembled into a three-dimensional hydrogen-bonding network by N—H⋯O hydrogen bonds. |
format | Online Article Text |
id | pubmed-3247435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32474352012-01-04 meso-3,6-Dioxopiperazine-2,5-diacetamide Li, Ping Zhang, Chun Xu, Wei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(12)N(4)O(4), was obtained by cyclization of the two l-asparagine molecules and reveals a crystallographic inversion symmetry, and accordingly the two stereogenic centres are of opposite chirality. Thus, an asymmetric unit comprises a half of a molecule. The molecules are assembled into a three-dimensional hydrogen-bonding network by N—H⋯O hydrogen bonds. International Union of Crystallography 2011-10-29 /pmc/articles/PMC3247435/ /pubmed/22220053 http://dx.doi.org/10.1107/S1600536811043376 Text en © Li et al. 2011 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, Ping Zhang, Chun Xu, Wei meso-3,6-Dioxopiperazine-2,5-diacetamide |
title |
meso-3,6-Dioxopiperazine-2,5-diacetamide |
title_full |
meso-3,6-Dioxopiperazine-2,5-diacetamide |
title_fullStr |
meso-3,6-Dioxopiperazine-2,5-diacetamide |
title_full_unstemmed |
meso-3,6-Dioxopiperazine-2,5-diacetamide |
title_short |
meso-3,6-Dioxopiperazine-2,5-diacetamide |
title_sort | meso-3,6-dioxopiperazine-2,5-diacetamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247435/ https://www.ncbi.nlm.nih.gov/pubmed/22220053 http://dx.doi.org/10.1107/S1600536811043376 |
work_keys_str_mv | AT liping meso36dioxopiperazine25diacetamide AT zhangchun meso36dioxopiperazine25diacetamide AT xuwei meso36dioxopiperazine25diacetamide |