(S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone
The title compound, C16H18ClNO3, was obtained by the organocatalytic asymmetric Michael addition of cyclohexanone to 1-chloro-4-[(1E,3E)-4-nitrobuta-1,3-dienyl]benzene. The double bond has an E configuration. The cyclohexanone ring adopts a chair conformation. The conformation of the molecule is sta...
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2009-08-01
|
| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536809029213 |
| _version_ | 1818791697686986752 |
|---|---|
| author | Zhaobo Li Yi Guo Bailin Li Shuping Luo |
| author_facet | Zhaobo Li Yi Guo Bailin Li Shuping Luo |
| author_sort | Zhaobo Li |
| collection | DOAJ |
| description | The title compound, C16H18ClNO3, was obtained by the organocatalytic asymmetric Michael addition of cyclohexanone to 1-chloro-4-[(1E,3E)-4-nitrobuta-1,3-dienyl]benzene. The double bond has an E configuration. The cyclohexanone ring adopts a chair conformation. The conformation of the molecule is stabilized by a weak intramolecular C—H...O hydrogen bond. |
| first_indexed | 2024-12-18T15:15:28Z |
| format | Article |
| id | doaj.art-9d47bbc1d9824da0bb0499c139d4880c |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-18T15:15:28Z |
| publishDate | 2009-08-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-9d47bbc1d9824da0bb0499c139d4880c2022-12-21T21:03:32ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-08-01658o2023o202310.1107/S1600536809029213(S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanoneZhaobo LiYi GuoBailin LiShuping LuoThe title compound, C16H18ClNO3, was obtained by the organocatalytic asymmetric Michael addition of cyclohexanone to 1-chloro-4-[(1E,3E)-4-nitrobuta-1,3-dienyl]benzene. The double bond has an E configuration. The cyclohexanone ring adopts a chair conformation. The conformation of the molecule is stabilized by a weak intramolecular C—H...O hydrogen bond.http://scripts.iucr.org/cgi-bin/paper?S1600536809029213 |
| spellingShingle | Zhaobo Li Yi Guo Bailin Li Shuping Luo (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone Acta Crystallographica Section E |
| title | (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone |
| title_full | (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone |
| title_fullStr | (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone |
| title_full_unstemmed | (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone |
| title_short | (S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone |
| title_sort | s 2 s e 4 4 chlorophenyl 1 nitrobut 3 en 2 yl cyclohexanone |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536809029213 |
| work_keys_str_mv | AT zhaoboli s2se44chlorophenyl1nitrobut3en2ylcyclohexanone AT yiguo s2se44chlorophenyl1nitrobut3en2ylcyclohexanone AT bailinli s2se44chlorophenyl1nitrobut3en2ylcyclohexanone AT shupingluo s2se44chlorophenyl1nitrobut3en2ylcyclohexanone |