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Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide
The degradation of atorvastatin calcium in methanol and hydrogen peroxide results in the crystallization of the title compound, C(26)H(24)FNO(6), which shows several differences compared with the starting compound. In the crystal structure of the title compound, intra- and intermolecular hydrogen b...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962052/ https://www.ncbi.nlm.nih.gov/pubmed/21203252 http://dx.doi.org/10.1107/S1600536808022265 |
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author | Ashfaq, Muhammad Tahir, Muhammad Nawaz Khan, Islam Ullah Iqbal, Mohammad S. Arshad, Muhammad Nadeem |
author_facet | Ashfaq, Muhammad Tahir, Muhammad Nawaz Khan, Islam Ullah Iqbal, Mohammad S. Arshad, Muhammad Nadeem |
author_sort | Ashfaq, Muhammad |
collection | PubMed |
description | The degradation of atorvastatin calcium in methanol and hydrogen peroxide results in the crystallization of the title compound, C(26)H(24)FNO(6), which shows several differences compared with the starting compound. In the crystal structure of the title compound, intra- and intermolecular hydrogen bonding is found. |
format | Text |
id | pubmed-2962052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29620522010-12-30 Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide Ashfaq, Muhammad Tahir, Muhammad Nawaz Khan, Islam Ullah Iqbal, Mohammad S. Arshad, Muhammad Nadeem Acta Crystallogr Sect E Struct Rep Online Organic Papers The degradation of atorvastatin calcium in methanol and hydrogen peroxide results in the crystallization of the title compound, C(26)H(24)FNO(6), which shows several differences compared with the starting compound. In the crystal structure of the title compound, intra- and intermolecular hydrogen bonding is found. International Union of Crystallography 2008-07-19 /pmc/articles/PMC2962052/ /pubmed/21203252 http://dx.doi.org/10.1107/S1600536808022265 Text en © Ashfaq 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 Ashfaq, Muhammad Tahir, Muhammad Nawaz Khan, Islam Ullah Iqbal, Mohammad S. Arshad, Muhammad Nadeem Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title | Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title_full | Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title_fullStr | Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title_full_unstemmed | Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title_short | Degradation of atorvastatin: (1R,2S,4S,5S)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-N,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
title_sort | degradation of atorvastatin: (1r,2s,4s,5s)-4-(4-fluorophenyl)-2-hydroperoxy-4-hydroxy-2-isopropyl-n,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-1-carboxamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962052/ https://www.ncbi.nlm.nih.gov/pubmed/21203252 http://dx.doi.org/10.1107/S1600536808022265 |
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