E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate

The title compound, C(21)H(21)ClO(7)·C(2)H(5)OH was synthesized by the condensation reaction between helicid [systematic name: 4-(β-d-allopyranos­yloxy)benzaldehyde] and 4-chloro­aceto­phen­one in ethanol. In the mol­ecular structure, the pyran­oside ring adopts a chair conformation. In the crystal...

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Detalles Bibliográficos
Autores principales: Yang, Cong-ling, Luo, Hua-ling, Yin, Xiu-juan, Li, Ying, Yin, Shu-fan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968659/
https://www.ncbi.nlm.nih.gov/pubmed/21582283
http://dx.doi.org/10.1107/S1600536809006424
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author Yang, Cong-ling
Luo, Hua-ling
Yin, Xiu-juan
Li, Ying
Yin, Shu-fan
author_facet Yang, Cong-ling
Luo, Hua-ling
Yin, Xiu-juan
Li, Ying
Yin, Shu-fan
author_sort Yang, Cong-ling
collection PubMed
description The title compound, C(21)H(21)ClO(7)·C(2)H(5)OH was synthesized by the condensation reaction between helicid [systematic name: 4-(β-d-allopyranos­yloxy)benzaldehyde] and 4-chloro­aceto­phen­one in ethanol. In the mol­ecular structure, the pyran­oside ring adopts a chair conformation. In the crystal structure, the molecules are linked by inter­molecular O—H⋯O hydrogen bonds involving the OH groups from the pyran­oside unit and from the ethanol solvent mol­ecule.
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spelling pubmed-29686592010-12-30 E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate Yang, Cong-ling Luo, Hua-ling Yin, Xiu-juan Li, Ying Yin, Shu-fan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(21)ClO(7)·C(2)H(5)OH was synthesized by the condensation reaction between helicid [systematic name: 4-(β-d-allopyranos­yloxy)benzaldehyde] and 4-chloro­aceto­phen­one in ethanol. In the mol­ecular structure, the pyran­oside ring adopts a chair conformation. In the crystal structure, the molecules are linked by inter­molecular O—H⋯O hydrogen bonds involving the OH groups from the pyran­oside unit and from the ethanol solvent mol­ecule. International Union of Crystallography 2009-02-28 /pmc/articles/PMC2968659/ /pubmed/21582283 http://dx.doi.org/10.1107/S1600536809006424 Text en © Yang et al. 2009 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
Yang, Cong-ling
Luo, Hua-ling
Yin, Xiu-juan
Li, Ying
Yin, Shu-fan
E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title_full E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title_fullStr E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title_full_unstemmed E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title_short E-[4-(β-d-Allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
title_sort e-[4-(β-d-allopyranos­yloxy)phen­yl]-1-(4-chloro­phen­yl)prop-2-enone ethanol solvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968659/
https://www.ncbi.nlm.nih.gov/pubmed/21582283
http://dx.doi.org/10.1107/S1600536809006424
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