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(4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione
In the title compound, C(37)H(27)Cl(2)NO(2), the 3,4-dichlorophenyl ring makes a dihedral angle of 46.66 (6)° with the phenyl ring. The molecular structure is stabilized by weak intramolecular C—H⋯O interactions and the crystal structure is stabilized by weak intermolecular C—H⋯O interactions....
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961525/ https://www.ncbi.nlm.nih.gov/pubmed/21202604 http://dx.doi.org/10.1107/S1600536808013846 |
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author | Murugan, R. Gunasekaran, B. Narayanan, S. Sriman Manivannan, V. |
author_facet | Murugan, R. Gunasekaran, B. Narayanan, S. Sriman Manivannan, V. |
author_sort | Murugan, R. |
collection | PubMed |
description | In the title compound, C(37)H(27)Cl(2)NO(2), the 3,4-dichlorophenyl ring makes a dihedral angle of 46.66 (6)° with the phenyl ring. The molecular structure is stabilized by weak intramolecular C—H⋯O interactions and the crystal structure is stabilized by weak intermolecular C—H⋯O interactions. The C–C–C–C–C five-membered ring is planar, while the C–C–C–C–N five-membered ring adopts a half-chair conformation. |
format | Text |
id | pubmed-2961525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29615252010-12-30 (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione Murugan, R. Gunasekaran, B. Narayanan, S. Sriman Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(37)H(27)Cl(2)NO(2), the 3,4-dichlorophenyl ring makes a dihedral angle of 46.66 (6)° with the phenyl ring. The molecular structure is stabilized by weak intramolecular C—H⋯O interactions and the crystal structure is stabilized by weak intermolecular C—H⋯O interactions. The C–C–C–C–C five-membered ring is planar, while the C–C–C–C–N five-membered ring adopts a half-chair conformation. International Union of Crystallography 2008-05-17 /pmc/articles/PMC2961525/ /pubmed/21202604 http://dx.doi.org/10.1107/S1600536808013846 Text en © Murugan 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 Murugan, R. Gunasekaran, B. Narayanan, S. Sriman Manivannan, V. (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title | (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title_full | (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title_fullStr | (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title_full_unstemmed | (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title_short | (4S)-4-(3,4-Dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2H,1′′H)-dione |
title_sort | (4s)-4-(3,4-dichlorophenyl)-1′-methyl-4′-phenyl-3,4-dihydronaphthalene-2-spiro-3′-pyrrolidine-2′-spiro-1′′-acenaphthylene-1,2′′(2h,1′′h)-dione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961525/ https://www.ncbi.nlm.nih.gov/pubmed/21202604 http://dx.doi.org/10.1107/S1600536808013846 |
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