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(E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine
The title compound, C(27)H(34)ClN, has been synthesized from 4-chlorobenzaldehyde and dehydroabietylamine. There are two unique molecules in the unit cell. Each molecule has three chiral centres, which exhibit R, S and R absolute configurations. The two cyclohexane rings form a trans ring junct...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977794/ https://www.ncbi.nlm.nih.gov/pubmed/21583930 http://dx.doi.org/10.1107/S1600536809013245 |
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author | Chen, Yu-Xiang Zhao, Zhen-Dong Wang, Yu-Min Bi, Liang-Wu |
author_facet | Chen, Yu-Xiang Zhao, Zhen-Dong Wang, Yu-Min Bi, Liang-Wu |
author_sort | Chen, Yu-Xiang |
collection | PubMed |
description | The title compound, C(27)H(34)ClN, has been synthesized from 4-chlorobenzaldehyde and dehydroabietylamine. There are two unique molecules in the unit cell. Each molecule has three chiral centres, which exhibit R, S and R absolute configurations. The two cyclohexane rings form a trans ring junction with classical chair and half-chair conformations. |
format | Text |
id | pubmed-2977794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29777942010-12-30 (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine Chen, Yu-Xiang Zhao, Zhen-Dong Wang, Yu-Min Bi, Liang-Wu Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(27)H(34)ClN, has been synthesized from 4-chlorobenzaldehyde and dehydroabietylamine. There are two unique molecules in the unit cell. Each molecule has three chiral centres, which exhibit R, S and R absolute configurations. The two cyclohexane rings form a trans ring junction with classical chair and half-chair conformations. International Union of Crystallography 2009-04-25 /pmc/articles/PMC2977794/ /pubmed/21583930 http://dx.doi.org/10.1107/S1600536809013245 Text en © Chen et al. 2009 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 Chen, Yu-Xiang Zhao, Zhen-Dong Wang, Yu-Min Bi, Liang-Wu (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title | (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title_full | (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title_fullStr | (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title_full_unstemmed | (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title_short | (E)-(4-Chlorobenzylidene){[(1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
title_sort | (e)-(4-chlorobenzylidene){[(1r,4as,10ar)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthryl]methyl}amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977794/ https://www.ncbi.nlm.nih.gov/pubmed/21583930 http://dx.doi.org/10.1107/S1600536809013245 |
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