(Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one

The title compound, C(17)H(13)NO, synthesized to be tested for neuroprotective activities, consists of an indoline and a phenyl­allyl­idene unit with a dihedral angle of 9.0 (1)° between the two ring systems. There are two independent mol­ecules in the asymmetric unit which are connected into a dime...

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Detalles Bibliográficos
Autores principales: Zhang, Hongming, Akubathini, Shashidhar Kumar, Ankati, Haribabu, Biehl, Ed
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968140/
https://www.ncbi.nlm.nih.gov/pubmed/21581961
http://dx.doi.org/10.1107/S1600536809002037
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author Zhang, Hongming
Akubathini, Shashidhar Kumar
Ankati, Haribabu
Biehl, Ed
author_facet Zhang, Hongming
Akubathini, Shashidhar Kumar
Ankati, Haribabu
Biehl, Ed
author_sort Zhang, Hongming
collection PubMed
description The title compound, C(17)H(13)NO, synthesized to be tested for neuroprotective activities, consists of an indoline and a phenyl­allyl­idene unit with a dihedral angle of 9.0 (1)° between the two ring systems. There are two independent mol­ecules in the asymmetric unit which are connected into a dimer by inter­molecular N—H⋯O hydrogen bonds.
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spelling pubmed-29681402010-12-30 (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one Zhang, Hongming Akubathini, Shashidhar Kumar Ankati, Haribabu Biehl, Ed Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(13)NO, synthesized to be tested for neuroprotective activities, consists of an indoline and a phenyl­allyl­idene unit with a dihedral angle of 9.0 (1)° between the two ring systems. There are two independent mol­ecules in the asymmetric unit which are connected into a dimer by inter­molecular N—H⋯O hydrogen bonds. International Union of Crystallography 2009-01-23 /pmc/articles/PMC2968140/ /pubmed/21581961 http://dx.doi.org/10.1107/S1600536809002037 Text en © Zhang et al. 2009 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
Zhang, Hongming
Akubathini, Shashidhar Kumar
Ankati, Haribabu
Biehl, Ed
(Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title_full (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title_fullStr (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title_full_unstemmed (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title_short (Z)-3-[(E)-3-Phenyl­allyl­idene]indolin-2-one
title_sort (z)-3-[(e)-3-phenyl­allyl­idene]indolin-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968140/
https://www.ncbi.nlm.nih.gov/pubmed/21581961
http://dx.doi.org/10.1107/S1600536809002037
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AT biehled z3e3phenylallylideneindolin2one

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