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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...

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Detalles Bibliográficos
Autores principales: Lopchuk, Justin M., Gribble, Gordon W., Jasinski, Jerry P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
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].
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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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