N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide

In the title racemic compound, C(14)H(10)ClNO(3), which contains four stereogenic centres, the cyclo­hexane ring tends towards a boat conformation, while the tetra­hydro­furan and dihydro­furan rings adopt envelope conformations. The dihedral angle between the mean planes of the pyrrolidine-2,5-dion...

Descripción completa

Detalles Bibliográficos
Autor principal: Li, Jian
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011550/
https://www.ncbi.nlm.nih.gov/pubmed/21589527
http://dx.doi.org/10.1107/S1600536810047537
_version_ 1782194968721358848
author Li, Jian
author_facet Li, Jian
author_sort Li, Jian
collection PubMed
description In the title racemic compound, C(14)H(10)ClNO(3), which contains four stereogenic centres, the cyclo­hexane ring tends towards a boat conformation, while the tetra­hydro­furan and dihydro­furan rings adopt envelope conformations. The dihedral angle between the mean planes of the pyrrolidine-2,5-dione unit and the 4-chloro­phenyl ring is 49.0 (2)°.
format Text
id pubmed-3011550
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30115502010-12-30 N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide Li, Jian Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title racemic compound, C(14)H(10)ClNO(3), which contains four stereogenic centres, the cyclo­hexane ring tends towards a boat conformation, while the tetra­hydro­furan and dihydro­furan rings adopt envelope conformations. The dihedral angle between the mean planes of the pyrrolidine-2,5-dione unit and the 4-chloro­phenyl ring is 49.0 (2)°. International Union of Crystallography 2010-11-20 /pmc/articles/PMC3011550/ /pubmed/21589527 http://dx.doi.org/10.1107/S1600536810047537 Text en © Jian Li 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
Li, Jian
N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title_full N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title_fullStr N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title_full_unstemmed N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title_short N-(4-Chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
title_sort n-(4-chloro­phen­yl)-7-oxabicyclo­[2.2.1]hept-5-ene-2,3-dicarboximide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011550/
https://www.ncbi.nlm.nih.gov/pubmed/21589527
http://dx.doi.org/10.1107/S1600536810047537
work_keys_str_mv AT lijian n4chlorophenyl7oxabicyclo221hept5ene23dicarboximide

Ejemplares similares