trans-Ethyl­enedi-p-phenyl­ene diacetate

The centrosymmetric title compound, C(18)H(26)O(4), was prepared in high yield from 4-acetoxy­styrene via Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. In the crystal, a strong C—H⋯π inter­molecular inter­action links the mol­ecules together....

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Detalles Bibliográficos
Autores principales: Ritter, Stefanie, Neudörfl, Jörg-M., Velder, Janna, Schmalz, Hans-Günther
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970084/
https://www.ncbi.nlm.nih.gov/pubmed/21577628
http://dx.doi.org/10.1107/S1600536809032620
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author Ritter, Stefanie
Neudörfl, Jörg-M.
Velder, Janna
Schmalz, Hans-Günther
author_facet Ritter, Stefanie
Neudörfl, Jörg-M.
Velder, Janna
Schmalz, Hans-Günther
author_sort Ritter, Stefanie
collection PubMed
description The centrosymmetric title compound, C(18)H(26)O(4), was prepared in high yield from 4-acetoxy­styrene via Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. In the crystal, a strong C—H⋯π inter­molecular inter­action links the mol­ecules together.
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spelling pubmed-29700842010-12-30 trans-Ethyl­enedi-p-phenyl­ene diacetate Ritter, Stefanie Neudörfl, Jörg-M. Velder, Janna Schmalz, Hans-Günther Acta Crystallogr Sect E Struct Rep Online Organic Papers The centrosymmetric title compound, C(18)H(26)O(4), was prepared in high yield from 4-acetoxy­styrene via Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. In the crystal, a strong C—H⋯π inter­molecular inter­action links the mol­ecules together. International Union of Crystallography 2009-08-26 /pmc/articles/PMC2970084/ /pubmed/21577628 http://dx.doi.org/10.1107/S1600536809032620 Text en © Ritter 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
Ritter, Stefanie
Neudörfl, Jörg-M.
Velder, Janna
Schmalz, Hans-Günther
trans-Ethyl­enedi-p-phenyl­ene diacetate
title trans-Ethyl­enedi-p-phenyl­ene diacetate
title_full trans-Ethyl­enedi-p-phenyl­ene diacetate
title_fullStr trans-Ethyl­enedi-p-phenyl­ene diacetate
title_full_unstemmed trans-Ethyl­enedi-p-phenyl­ene diacetate
title_short trans-Ethyl­enedi-p-phenyl­ene diacetate
title_sort trans-ethyl­enedi-p-phenyl­ene diacetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970084/
https://www.ncbi.nlm.nih.gov/pubmed/21577628
http://dx.doi.org/10.1107/S1600536809032620
work_keys_str_mv AT ritterstefanie transethylenedipphenylenediacetate
AT neudorfljorgm transethylenedipphenylenediacetate
AT velderjanna transethylenedipphenylenediacetate
AT schmalzhansgunther transethylenedipphenylenediacetate

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