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(±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione
In the title compound, C(19)H(30)O(3)Si, both rings adopt a half-boat conformation. Overall, the molecule approximates a U-shape as the cyclo-2-ene-1,4-dione and butyldimethylsilyloxy substituents lie to the same side of the central cyclohexene ring; the methyl substituent lies to the other sid...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588414/ https://www.ncbi.nlm.nih.gov/pubmed/23476523 http://dx.doi.org/10.1107/S1600536813002973 |
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author | Delling, Felix N. Zukerman-Schpector, Julio Brocksom, Timothy J. Brocksom, Ursula Finelli, Fernanda G. Tiekink, Edward R. T. |
author_facet | Delling, Felix N. Zukerman-Schpector, Julio Brocksom, Timothy J. Brocksom, Ursula Finelli, Fernanda G. Tiekink, Edward R. T. |
author_sort | Delling, Felix N. |
collection | PubMed |
description | In the title compound, C(19)H(30)O(3)Si, both rings adopt a half-boat conformation. Overall, the molecule approximates a U-shape as the cyclo-2-ene-1,4-dione and butyldimethylsilyloxy substituents lie to the same side of the central cyclohexene ring; the methyl substituent lies to the other side of the molecule. In the crystal, linear supramolecular chains along the b axis are sustained by C—H⋯O interactions. |
format | Online Article Text |
id | pubmed-3588414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35884142013-03-08 (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione Delling, Felix N. Zukerman-Schpector, Julio Brocksom, Timothy J. Brocksom, Ursula Finelli, Fernanda G. Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(30)O(3)Si, both rings adopt a half-boat conformation. Overall, the molecule approximates a U-shape as the cyclo-2-ene-1,4-dione and butyldimethylsilyloxy substituents lie to the same side of the central cyclohexene ring; the methyl substituent lies to the other side of the molecule. In the crystal, linear supramolecular chains along the b axis are sustained by C—H⋯O interactions. International Union of Crystallography 2013-02-02 /pmc/articles/PMC3588414/ /pubmed/23476523 http://dx.doi.org/10.1107/S1600536813002973 Text en © Delling et al. 2013 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 Delling, Felix N. Zukerman-Schpector, Julio Brocksom, Timothy J. Brocksom, Ursula Finelli, Fernanda G. Tiekink, Edward R. T. (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title | (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title_full | (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title_fullStr | (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title_full_unstemmed | (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title_short | (±)-(4aR,5R,8S,8aR)-8-(tert-Butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
title_sort | (±)-(4ar,5r,8s,8ar)-8-(tert-butyldimethylsilyloxy)-2,5,8a-trimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588414/ https://www.ncbi.nlm.nih.gov/pubmed/23476523 http://dx.doi.org/10.1107/S1600536813002973 |
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