(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one
In the title compound, C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation. The chiral crystals were obtained from a racemic reaction product via spontaneous resolution.
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2012-06-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812020065 |
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doaj-e288e044db4b4827a4dc3d08ca4f2e45 |
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Article |
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doaj-e288e044db4b4827a4dc3d08ca4f2e452020-11-25T03:05:24ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-06-01686o1691o169110.1107/S1600536812020065(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-oneZhen-ju JiangQi HeZhen LiZhou-yu WangIn the title compound, C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation. The chiral crystals were obtained from a racemic reaction product via spontaneous resolution.http://scripts.iucr.org/cgi-bin/paper?S1600536812020065 |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Zhen-ju Jiang Qi He Zhen Li Zhou-yu Wang |
| spellingShingle |
Zhen-ju Jiang Qi He Zhen Li Zhou-yu Wang (1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one Acta Crystallographica Section E |
| author_facet |
Zhen-ju Jiang Qi He Zhen Li Zhou-yu Wang |
| author_sort |
Zhen-ju Jiang |
| title |
(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| title_short |
(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| title_full |
(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| title_fullStr |
(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| title_full_unstemmed |
(1S*,5R*)-9-Phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| title_sort |
(1s*,5r*)-9-phenyl-9-azabicyclo[3.3.1]nonan-3-one |
| publisher |
International Union of Crystallography |
| series |
Acta Crystallographica Section E |
| issn |
1600-5368 |
| publishDate |
2012-06-01 |
| description |
In the title compound, C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation. The chiral crystals were obtained from a racemic reaction product via spontaneous resolution. |
| url |
http://scripts.iucr.org/cgi-bin/paper?S1600536812020065 |
| work_keys_str_mv |
AT zhenjujiang 1s5r9phenyl9azabicyclo331nonan3one AT qihe 1s5r9phenyl9azabicyclo331nonan3one AT zhenli 1s5r9phenyl9azabicyclo331nonan3one AT zhouyuwang 1s5r9phenyl9azabicyclo331nonan3one |
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