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(1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one

In the title compound, C(33)H(32)N(2)O(2), the polysubstituted piperidine ring adopts a chair conformation. The isoxazolidine ring is in an envelope conformation. In the crystal structure, intra- and inter­molecular C—H⋯π inter­actions involving the phenyl rings are observed.

Detalles Bibliográficos
Autores principales: Malathy, A., Kumar, R. Suresh, Perumal, S., Suresh, J., Lakshman, Nilantha
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915384/
https://www.ncbi.nlm.nih.gov/pubmed/21200905
http://dx.doi.org/10.1107/S1600536807067256
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author Malathy, A.
Kumar, R. Suresh
Perumal, S.
Suresh, J.
Lakshman, Nilantha
author_facet Malathy, A.
Kumar, R. Suresh
Perumal, S.
Suresh, J.
Lakshman, Nilantha
author_sort Malathy, A.
collection PubMed
description In the title compound, C(33)H(32)N(2)O(2), the polysubstituted piperidine ring adopts a chair conformation. The isoxazolidine ring is in an envelope conformation. In the crystal structure, intra- and inter­molecular C—H⋯π inter­actions involving the phenyl rings are observed.
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spelling pubmed-29153842010-12-30 (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one Malathy, A. Kumar, R. Suresh Perumal, S. Suresh, J. Lakshman, Nilantha Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(33)H(32)N(2)O(2), the polysubstituted piperidine ring adopts a chair conformation. The isoxazolidine ring is in an envelope conformation. In the crystal structure, intra- and inter­molecular C—H⋯π inter­actions involving the phenyl rings are observed. International Union of Crystallography 2007-12-21 /pmc/articles/PMC2915384/ /pubmed/21200905 http://dx.doi.org/10.1107/S1600536807067256 Text en © Malathy 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
Malathy, A.
Kumar, R. Suresh
Perumal, S.
Suresh, J.
Lakshman, Nilantha
(1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title_full (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title_fullStr (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title_full_unstemmed (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title_short (1R,4R,5R)-1,3,4-Triphenyl-7-[(R)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
title_sort (1r,4r,5r)-1,3,4-triphenyl-7-[(r)-1-phenyl­ethyl]-2-oxa-3,7-diaza­spiro­[4.5]decan-10-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915384/
https://www.ncbi.nlm.nih.gov/pubmed/21200905
http://dx.doi.org/10.1107/S1600536807067256
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