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Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate
In the title compound, C(11)H(17)NO(4), commonly known as N-tert-butoxycarbonyl-5-hydroxy-d-pipecolic acid lactone, the absolute configuration is (1R,4R) due to the enantiomeric purity of the starting material which remains unchanged during the course of the reaction. In the crystal there no inte...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518923/ https://www.ncbi.nlm.nih.gov/pubmed/26279901 http://dx.doi.org/10.1107/S2056989015010476 |
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author | Krishnamurthy, Suvratha Jalli, Venkataprasad Vagvala, Tarun Chand Moriguchi, Tetsuji Tsuge, Akihiko |
author_facet | Krishnamurthy, Suvratha Jalli, Venkataprasad Vagvala, Tarun Chand Moriguchi, Tetsuji Tsuge, Akihiko |
author_sort | Krishnamurthy, Suvratha |
collection | PubMed |
description | In the title compound, C(11)H(17)NO(4), commonly known as N-tert-butoxycarbonyl-5-hydroxy-d-pipecolic acid lactone, the absolute configuration is (1R,4R) due to the enantiomeric purity of the starting material which remains unchanged during the course of the reaction. In the crystal there no intermolecular hydrogen bonds. |
format | Online Article Text |
id | pubmed-4518923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-45189232015-08-14 Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate Krishnamurthy, Suvratha Jalli, Venkataprasad Vagvala, Tarun Chand Moriguchi, Tetsuji Tsuge, Akihiko Acta Crystallogr E Crystallogr Commun Data Reports In the title compound, C(11)H(17)NO(4), commonly known as N-tert-butoxycarbonyl-5-hydroxy-d-pipecolic acid lactone, the absolute configuration is (1R,4R) due to the enantiomeric purity of the starting material which remains unchanged during the course of the reaction. In the crystal there no intermolecular hydrogen bonds. International Union of Crystallography 2015-06-06 /pmc/articles/PMC4518923/ /pubmed/26279901 http://dx.doi.org/10.1107/S2056989015010476 Text en © Krishnamurthy et al. 2015 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 | Data Reports Krishnamurthy, Suvratha Jalli, Venkataprasad Vagvala, Tarun Chand Moriguchi, Tetsuji Tsuge, Akihiko Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title | Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title_full | Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title_fullStr | Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title_full_unstemmed | Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title_short | Crystal structure of (1R,4R)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
title_sort | crystal structure of (1r,4r)-tert-butyl 3-oxo-2-oxa-5-azabicyclo[2.2.2]octane-5-carboxylate |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518923/ https://www.ncbi.nlm.nih.gov/pubmed/26279901 http://dx.doi.org/10.1107/S2056989015010476 |
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