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3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol

In the title compound, C(27)H(21)NO(2), the half-chair conformation of the alicyclic rings gives rise to a slightly folded structure of the central tricyclic tetra­hydrophenanthridine unit. Tandem intra­molecular O—H⋯N and O—H⋯O hydrogen bonds give rise to adjacent S(6) and S(5) rings, respectively,...

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Autores principales: Karthikeyan, N. S., Ramachandran, G., Sathiyanarayanan, K., Raghavaiah, P., Rathore, R. S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007033/
https://www.ncbi.nlm.nih.gov/pubmed/21587969
http://dx.doi.org/10.1107/S1600536810023688
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author Karthikeyan, N. S.
Ramachandran, G.
Sathiyanarayanan, K.
Raghavaiah, P.
Rathore, R. S.
author_facet Karthikeyan, N. S.
Ramachandran, G.
Sathiyanarayanan, K.
Raghavaiah, P.
Rathore, R. S.
author_sort Karthikeyan, N. S.
collection PubMed
description In the title compound, C(27)H(21)NO(2), the half-chair conformation of the alicyclic rings gives rise to a slightly folded structure of the central tricyclic tetra­hydrophenanthridine unit. Tandem intra­molecular O—H⋯N and O—H⋯O hydrogen bonds give rise to adjacent S(6) and S(5) rings, respectively, which dictate the conformation of the 5-aryl substituent. In the crystal structure, an inter­molecular C—H⋯O contact generates chains parallel to [101]. Short O—H⋯π and C—H⋯π contacts are also observed.
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spelling pubmed-30070332010-12-30 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol Karthikeyan, N. S. Ramachandran, G. Sathiyanarayanan, K. Raghavaiah, P. Rathore, R. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(21)NO(2), the half-chair conformation of the alicyclic rings gives rise to a slightly folded structure of the central tricyclic tetra­hydrophenanthridine unit. Tandem intra­molecular O—H⋯N and O—H⋯O hydrogen bonds give rise to adjacent S(6) and S(5) rings, respectively, which dictate the conformation of the 5-aryl substituent. In the crystal structure, an inter­molecular C—H⋯O contact generates chains parallel to [101]. Short O—H⋯π and C—H⋯π contacts are also observed. International Union of Crystallography 2010-06-23 /pmc/articles/PMC3007033/ /pubmed/21587969 http://dx.doi.org/10.1107/S1600536810023688 Text en © Karthikeyan 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
Karthikeyan, N. S.
Ramachandran, G.
Sathiyanarayanan, K.
Raghavaiah, P.
Rathore, R. S.
3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title_full 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title_fullStr 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title_full_unstemmed 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title_short 3-(7,8,13,14-Tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
title_sort 3-(7,8,13,14-tetra­hydrodi­benzo­[a,i]phen­an­thridin-5-yl)benzene-1,2-diol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007033/
https://www.ncbi.nlm.nih.gov/pubmed/21587969
http://dx.doi.org/10.1107/S1600536810023688
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