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3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole

In the title compound, C(17)H(17)NO(3), the five-membered isoxazoline ring adopts an envelope conformation with the chiral C atom at the flap position and 0.133 (2) Å out of the mean plane formed by the other four atoms. The two benzene rings form dihedral angles of 6.05 (5) and 81.52 (5)° with the...

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Detalles Bibliográficos
Autores principales: Samshuddin, S., Butcher, Ray J., Akkurt, Mehmet, Narayana, B., Yathirajan, H. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213434/
https://www.ncbi.nlm.nih.gov/pubmed/22091013
http://dx.doi.org/10.1107/S1600536811026833
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author Samshuddin, S.
Butcher, Ray J.
Akkurt, Mehmet
Narayana, B.
Yathirajan, H. S.
author_facet Samshuddin, S.
Butcher, Ray J.
Akkurt, Mehmet
Narayana, B.
Yathirajan, H. S.
author_sort Samshuddin, S.
collection PubMed
description In the title compound, C(17)H(17)NO(3), the five-membered isoxazoline ring adopts an envelope conformation with the chiral C atom at the flap position and 0.133 (2) Å out of the mean plane formed by the other four atoms. The two benzene rings form dihedral angles of 6.05 (5) and 81.52 (5)° with the C—C—N—O plane of the isoxazoline ring. The crystal structure is stabilized by weak C—H⋯O hydrogen bonds and C—H⋯π inter­actions.
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spelling pubmed-32134342011-11-16 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole Samshuddin, S. Butcher, Ray J. Akkurt, Mehmet Narayana, B. Yathirajan, H. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(17)NO(3), the five-membered isoxazoline ring adopts an envelope conformation with the chiral C atom at the flap position and 0.133 (2) Å out of the mean plane formed by the other four atoms. The two benzene rings form dihedral angles of 6.05 (5) and 81.52 (5)° with the C—C—N—O plane of the isoxazoline ring. The crystal structure is stabilized by weak C—H⋯O hydrogen bonds and C—H⋯π inter­actions. International Union of Crystallography 2011-07-09 /pmc/articles/PMC3213434/ /pubmed/22091013 http://dx.doi.org/10.1107/S1600536811026833 Text en © Samshuddin 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
Samshuddin, S.
Butcher, Ray J.
Akkurt, Mehmet
Narayana, B.
Yathirajan, H. S.
3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title_full 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title_fullStr 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title_full_unstemmed 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title_short 3,5-Bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
title_sort 3,5-bis(4-meth­oxy­phen­yl)-4,5-dihydro­isoxazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213434/
https://www.ncbi.nlm.nih.gov/pubmed/22091013
http://dx.doi.org/10.1107/S1600536811026833
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