Cargando…
l-Nebiviololinium chloride dihydrate
The hydrochloride salt of chiral l-nebivolol {systematic name: (+)−(R,S,S,S)-bis[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxyethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(−)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate. The pyran rings adopt half...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915012/ https://www.ncbi.nlm.nih.gov/pubmed/21200930 http://dx.doi.org/10.1107/S1600536807061831 |
_version_ | 1782184838864830464 |
---|---|
author | Tuchalski, Gisbert Hänsicke, Andre Reck, Günther Emmerling, Franziska |
author_facet | Tuchalski, Gisbert Hänsicke, Andre Reck, Günther Emmerling, Franziska |
author_sort | Tuchalski, Gisbert |
collection | PubMed |
description | The hydrochloride salt of chiral l-nebivolol {systematic name: (+)−(R,S,S,S)-bis[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxyethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(−)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate. The pyran rings adopt half-chair conformations. Hydrogen bonds between the cation, anions and water molecules contribute to the formation of layers parallel to the ac plane. |
format | Text |
id | pubmed-2915012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29150122010-12-30 l-Nebiviololinium chloride dihydrate Tuchalski, Gisbert Hänsicke, Andre Reck, Günther Emmerling, Franziska Acta Crystallogr Sect E Struct Rep Online Organic Papers The hydrochloride salt of chiral l-nebivolol {systematic name: (+)−(R,S,S,S)-bis[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxyethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(−)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate. The pyran rings adopt half-chair conformations. Hydrogen bonds between the cation, anions and water molecules contribute to the formation of layers parallel to the ac plane. International Union of Crystallography 2007-12-06 /pmc/articles/PMC2915012/ /pubmed/21200930 http://dx.doi.org/10.1107/S1600536807061831 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html. |
spellingShingle | Organic Papers Tuchalski, Gisbert Hänsicke, Andre Reck, Günther Emmerling, Franziska l-Nebiviololinium chloride dihydrate |
title |
l-Nebiviololinium chloride dihydrate |
title_full |
l-Nebiviololinium chloride dihydrate |
title_fullStr |
l-Nebiviololinium chloride dihydrate |
title_full_unstemmed |
l-Nebiviololinium chloride dihydrate |
title_short |
l-Nebiviololinium chloride dihydrate |
title_sort | l-nebiviololinium chloride dihydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915012/ https://www.ncbi.nlm.nih.gov/pubmed/21200930 http://dx.doi.org/10.1107/S1600536807061831 |
work_keys_str_mv | AT tuchalskigisbert lnebiviololiniumchloridedihydrate AT hansickeandre lnebiviololiniumchloridedihydrate AT reckgunther lnebiviololiniumchloridedihydrate AT emmerlingfranziska lnebiviololiniumchloridedihydrate |