Cargando…

(S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none

In the crystal structure of the title compound, C(16)H(18)BrNO(3), the two stereogenic centres both have an S configuration. The cyclo­hexyl ring adopts a chair conformation. In the crystal, mol­ecules are linked by weak N—O⋯Br contacts [O⋯Br = 3.289 (4) Å].

Detalles Bibliográficos
Autores principales: Wu, Chao, Zhao, Long, Xia, Ai-Bao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212326/
https://www.ncbi.nlm.nih.gov/pubmed/22090983
http://dx.doi.org/10.1107/S1600536811025633
_version_ 1782215970161426432
author Wu, Chao
Zhao, Long
Xia, Ai-Bao
author_facet Wu, Chao
Zhao, Long
Xia, Ai-Bao
author_sort Wu, Chao
collection PubMed
description In the crystal structure of the title compound, C(16)H(18)BrNO(3), the two stereogenic centres both have an S configuration. The cyclo­hexyl ring adopts a chair conformation. In the crystal, mol­ecules are linked by weak N—O⋯Br contacts [O⋯Br = 3.289 (4) Å].
format Online
Article
Text
id pubmed-3212326
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32123262011-11-16 (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none Wu, Chao Zhao, Long Xia, Ai-Bao Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(16)H(18)BrNO(3), the two stereogenic centres both have an S configuration. The cyclo­hexyl ring adopts a chair conformation. In the crystal, mol­ecules are linked by weak N—O⋯Br contacts [O⋯Br = 3.289 (4) Å]. International Union of Crystallography 2011-07-06 /pmc/articles/PMC3212326/ /pubmed/22090983 http://dx.doi.org/10.1107/S1600536811025633 Text en © Wu 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
Wu, Chao
Zhao, Long
Xia, Ai-Bao
(S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title_full (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title_fullStr (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title_full_unstemmed (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title_short (S)-2-[(S,Z)-3-Bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
title_sort (s)-2-[(s,z)-3-bromo-1-nitro-4-phenyl­but-3-en-2-yl]cyclo­hexa­none
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212326/
https://www.ncbi.nlm.nih.gov/pubmed/22090983
http://dx.doi.org/10.1107/S1600536811025633
work_keys_str_mv AT wuchao s2sz3bromo1nitro4phenylbut3en2ylcyclohexanone
AT zhaolong s2sz3bromo1nitro4phenylbut3en2ylcyclohexanone
AT xiaaibao s2sz3bromo1nitro4phenylbut3en2ylcyclohexanone