Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one

In the title compound, C(13)H(22)N(2)O, the central imidazolidine ring is in an envelope conformation and the two cyclo­hexane rings adopt chair conformations. In the crystal structure, the mol­ecules are linked into centrosymmetric R (2) (2)(8) dimers by pairs of N—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Kavitha, T., Ponnuswamy, S., Vijayalakshmi, R., Thenmozhi, M., Ponnuswamy, M. N.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979210/
https://www.ncbi.nlm.nih.gov/pubmed/21579127
http://dx.doi.org/10.1107/S1600536810012468
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author Kavitha, T.
Ponnuswamy, S.
Vijayalakshmi, R.
Thenmozhi, M.
Ponnuswamy, M. N.
author_facet Kavitha, T.
Ponnuswamy, S.
Vijayalakshmi, R.
Thenmozhi, M.
Ponnuswamy, M. N.
author_sort Kavitha, T.
collection PubMed
description In the title compound, C(13)H(22)N(2)O, the central imidazolidine ring is in an envelope conformation and the two cyclo­hexane rings adopt chair conformations. In the crystal structure, the mol­ecules are linked into centrosymmetric R (2) (2)(8) dimers by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-29792102010-12-30 Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one Kavitha, T. Ponnuswamy, S. Vijayalakshmi, R. Thenmozhi, M. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(22)N(2)O, the central imidazolidine ring is in an envelope conformation and the two cyclo­hexane rings adopt chair conformations. In the crystal structure, the mol­ecules are linked into centrosymmetric R (2) (2)(8) dimers by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2010-04-14 /pmc/articles/PMC2979210/ /pubmed/21579127 http://dx.doi.org/10.1107/S1600536810012468 Text en © Kavitha et al. 2010 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
Kavitha, T.
Ponnuswamy, S.
Vijayalakshmi, R.
Thenmozhi, M.
Ponnuswamy, M. N.
Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title_full Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title_fullStr Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title_full_unstemmed Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title_short Cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
title_sort cyclo­hexane-1-spiro-2′-imidazolidine-5′-spiro-1′′-cyclo­hexan-4′-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979210/
https://www.ncbi.nlm.nih.gov/pubmed/21579127
http://dx.doi.org/10.1107/S1600536810012468
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AT thenmozhim cyclohexane1spiro2imidazolidine5spiro1cyclohexan4one
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