Cargando…

exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione

In the crystal of the title compound, C(10)H(11)NO(4), the hy­droxy group forms an O—H⋯O(carbon­yl) hydrogen bond with an adjacent molecule, so forming chains which extend along (010). Further weak C—H⋯O hydrogen-bonding associations give an infinite three-dimensional network structure.

Detalles Bibliográficos
Autores principales: Tan, Xue-Jie, Li, Chen-Guang, Xing, Dian-Xiang, Liu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297917/
https://www.ncbi.nlm.nih.gov/pubmed/22412720
http://dx.doi.org/10.1107/S160053681200788X
_version_ 1782225936900423680
author Tan, Xue-Jie
Li, Chen-Guang
Xing, Dian-Xiang
Liu, Yun
author_facet Tan, Xue-Jie
Li, Chen-Guang
Xing, Dian-Xiang
Liu, Yun
author_sort Tan, Xue-Jie
collection PubMed
description In the crystal of the title compound, C(10)H(11)NO(4), the hy­droxy group forms an O—H⋯O(carbon­yl) hydrogen bond with an adjacent molecule, so forming chains which extend along (010). Further weak C—H⋯O hydrogen-bonding associations give an infinite three-dimensional network structure.
format Online
Article
Text
id pubmed-3297917
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32979172012-03-12 exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione Tan, Xue-Jie Li, Chen-Guang Xing, Dian-Xiang Liu, Yun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title compound, C(10)H(11)NO(4), the hy­droxy group forms an O—H⋯O(carbon­yl) hydrogen bond with an adjacent molecule, so forming chains which extend along (010). Further weak C—H⋯O hydrogen-bonding associations give an infinite three-dimensional network structure. International Union of Crystallography 2012-02-29 /pmc/articles/PMC3297917/ /pubmed/22412720 http://dx.doi.org/10.1107/S160053681200788X Text en © Tan et al. 2012 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
Tan, Xue-Jie
Li, Chen-Guang
Xing, Dian-Xiang
Liu, Yun
exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title_full exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title_fullStr exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title_full_unstemmed exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title_short exo,exo-4-(2-Hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
title_sort exo,exo-4-(2-hy­droxy­eth­yl)-10-oxa-4-aza­tricyclo­[5.2.1.0(2,6)]dec-8-ene-3,5-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297917/
https://www.ncbi.nlm.nih.gov/pubmed/22412720
http://dx.doi.org/10.1107/S160053681200788X
work_keys_str_mv AT tanxuejie exoexo42hydroxyethyl10oxa4azatricyclo521026dec8ene35dione
AT lichenguang exoexo42hydroxyethyl10oxa4azatricyclo521026dec8ene35dione
AT xingdianxiang exoexo42hydroxyethyl10oxa4azatricyclo521026dec8ene35dione
AT liuyun exoexo42hydroxyethyl10oxa4azatricyclo521026dec8ene35dione