tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate

In the title compound, C(32)H(31)NO(4), the dihedral angles between the indoline ring and the two phenyl rings are 48.11 (9) and 66.55 (9)°. The mol­ecular conformation is stabilized by a weak intramolecular π–π stacking inter­action [centroid–centroid distance = 3.6377 (7) Å]. The crystal structure...

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Detalles Bibliográficos
Autores principales: Qiao, Zhen, Liu, Li, Wang, Dong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099990/
https://www.ncbi.nlm.nih.gov/pubmed/21754139
http://dx.doi.org/10.1107/S160053681100691X
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author Qiao, Zhen
Liu, Li
Wang, Dong
author_facet Qiao, Zhen
Liu, Li
Wang, Dong
author_sort Qiao, Zhen
collection PubMed
description In the title compound, C(32)H(31)NO(4), the dihedral angles between the indoline ring and the two phenyl rings are 48.11 (9) and 66.55 (9)°. The mol­ecular conformation is stabilized by a weak intramolecular π–π stacking inter­action [centroid–centroid distance = 3.6377 (7) Å]. The crystal structure is stabilized by inter­molecular C—H⋯O hydrogen bonds, which form chains along the b axis.
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spelling pubmed-30999902011-07-13 tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate Qiao, Zhen Liu, Li Wang, Dong Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(32)H(31)NO(4), the dihedral angles between the indoline ring and the two phenyl rings are 48.11 (9) and 66.55 (9)°. The mol­ecular conformation is stabilized by a weak intramolecular π–π stacking inter­action [centroid–centroid distance = 3.6377 (7) Å]. The crystal structure is stabilized by inter­molecular C—H⋯O hydrogen bonds, which form chains along the b axis. International Union of Crystallography 2011-03-12 /pmc/articles/PMC3099990/ /pubmed/21754139 http://dx.doi.org/10.1107/S160053681100691X Text en © Qiao et al. 2011 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
Qiao, Zhen
Liu, Li
Wang, Dong
tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title_full tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title_fullStr tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title_full_unstemmed tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title_short tert-Butyl 3-benzyl-3-[(E)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
title_sort tert-butyl 3-benzyl-3-[(e)-2-benzyl­idene-3-oxocyclo­pent­yl]-2-oxoindoline-1-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099990/
https://www.ncbi.nlm.nih.gov/pubmed/21754139
http://dx.doi.org/10.1107/S160053681100691X
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AT liuli tertbutyl3benzyl3e2benzylidene3oxocyclopentyl2oxoindoline1carboxylate
AT wangdong tertbutyl3benzyl3e2benzylidene3oxocyclopentyl2oxoindoline1carboxylate

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