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Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one
The title compound, C(13)H(13)NO, crystallizes with four independent molecules in the asymmetric unit. The 12-membered penta[b]indole rings are essentially planar, with maximum deviations ranging from 0.034 (4) to 0.036 (4) Å in the four unique molecules. In the crystal, weak C—H⋯O interactions...
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/PMC3772476/ https://www.ncbi.nlm.nih.gov/pubmed/24046619 http://dx.doi.org/10.1107/S1600536813014955 |
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author | Lopchuk, Justin M. Gribble, Gordon W. Jasinski, Jerry P. |
author_facet | Lopchuk, Justin M. Gribble, Gordon W. Jasinski, Jerry P. |
author_sort | Lopchuk, Justin M. |
collection | PubMed |
description | The title compound, C(13)H(13)NO, crystallizes with four independent molecules in the asymmetric unit. The 12-membered penta[b]indole rings are essentially planar, with maximum deviations ranging from 0.034 (4) to 0.036 (4) Å in the four unique molecules. In the crystal, weak C—H⋯O interactions are observed, which link the molecules into chains along [010]. |
format | Online Article Text |
id | pubmed-3772476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-37724762013-09-17 Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one Lopchuk, Justin M. Gribble, Gordon W. Jasinski, Jerry P. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(13)NO, crystallizes with four independent molecules in the asymmetric unit. The 12-membered penta[b]indole rings are essentially planar, with maximum deviations ranging from 0.034 (4) to 0.036 (4) Å in the four unique molecules. In the crystal, weak C—H⋯O interactions are observed, which link the molecules into chains along [010]. International Union of Crystallography 2013-06-08 /pmc/articles/PMC3772476/ /pubmed/24046619 http://dx.doi.org/10.1107/S1600536813014955 Text en © Lopchuk 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 Lopchuk, Justin M. Gribble, Gordon W. Jasinski, Jerry P. Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title | Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title_full | Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title_fullStr | Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title_full_unstemmed | Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title_short | Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one |
title_sort | bruceolline d: 3,3-dimethyl-1h,4h-cyclopenta[b]indol-2(3h)-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772476/ https://www.ncbi.nlm.nih.gov/pubmed/24046619 http://dx.doi.org/10.1107/S1600536813014955 |
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