(±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile

The furan ring in the title compound, C(26)H(18)N(2)O(2), is twisted about the C(H)—C(H) bond. The mol­ecular structure is stabilized by an intra­molecular C—H⋯O inter­action, which generates an S(6) ring motif. The presence of N—H⋯N hydrogen bonds leads to inversion dimers, which are stabilized in...

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Autores principales: Suresh, J., Vishnupriya, R., Gunasekaran, P., Perumal, S., Lakshman, P. L. Nilantha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344671/
https://www.ncbi.nlm.nih.gov/pubmed/22590433
http://dx.doi.org/10.1107/S1600536812018430
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author Suresh, J.
Vishnupriya, R.
Gunasekaran, P.
Perumal, S.
Lakshman, P. L. Nilantha
author_facet Suresh, J.
Vishnupriya, R.
Gunasekaran, P.
Perumal, S.
Lakshman, P. L. Nilantha
author_sort Suresh, J.
collection PubMed
description The furan ring in the title compound, C(26)H(18)N(2)O(2), is twisted about the C(H)—C(H) bond. The mol­ecular structure is stabilized by an intra­molecular C—H⋯O inter­action, which generates an S(6) ring motif. The presence of N—H⋯N hydrogen bonds leads to inversion dimers, which are stabilized in the crystal packing by C—H⋯O and C—H⋯π inter­actions, forming layers that stack along the a axis.
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spelling pubmed-33446712012-05-15 (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile Suresh, J. Vishnupriya, R. Gunasekaran, P. Perumal, S. Lakshman, P. L. Nilantha Acta Crystallogr Sect E Struct Rep Online Organic Papers The furan ring in the title compound, C(26)H(18)N(2)O(2), is twisted about the C(H)—C(H) bond. The mol­ecular structure is stabilized by an intra­molecular C—H⋯O inter­action, which generates an S(6) ring motif. The presence of N—H⋯N hydrogen bonds leads to inversion dimers, which are stabilized in the crystal packing by C—H⋯O and C—H⋯π inter­actions, forming layers that stack along the a axis. International Union of Crystallography 2012-04-28 /pmc/articles/PMC3344671/ /pubmed/22590433 http://dx.doi.org/10.1107/S1600536812018430 Text en © Suresh et al. 2012 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
Suresh, J.
Vishnupriya, R.
Gunasekaran, P.
Perumal, S.
Lakshman, P. L. Nilantha
(±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title_full (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title_fullStr (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title_full_unstemmed (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title_short (±)-trans-5-Benzoyl-2-(1H-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
title_sort (±)-trans-5-benzoyl-2-(1h-indol-3-yl)-4-phenyl-4,5-dihydro­furan-3-carbonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344671/
https://www.ncbi.nlm.nih.gov/pubmed/22590433
http://dx.doi.org/10.1107/S1600536812018430
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