trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene

The title compound, C(18)H(20)O(4), was prepared in high yield from 3,5-dimethoxy­styrene via a Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. Inter­estingly, one symmetric unit contains two mol­ecules adopting an s-syn-anti and and an all-s-anti...

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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/PMC2969882/
https://www.ncbi.nlm.nih.gov/pubmed/21577559
http://dx.doi.org/10.1107/S160053680903116X
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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 title compound, C(18)H(20)O(4), was prepared in high yield from 3,5-dimethoxy­styrene via a Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. Inter­estingly, one symmetric unit contains two mol­ecules adopting an s-syn-anti and and an all-s-anti conformation.
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spelling pubmed-29698822010-12-30 trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene Ritter, Stefanie Neudörfl, Jörg-M. Velder, Janna Schmalz, Hans-Günther Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(20)O(4), was prepared in high yield from 3,5-dimethoxy­styrene via a Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. Inter­estingly, one symmetric unit contains two mol­ecules adopting an s-syn-anti and and an all-s-anti conformation. International Union of Crystallography 2009-08-15 /pmc/articles/PMC2969882/ /pubmed/21577559 http://dx.doi.org/10.1107/S160053680903116X 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-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title_full trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title_fullStr trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title_full_unstemmed trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title_short trans-1,2-Bis(3,5-dimethoxy­phen­yl)ethene
title_sort trans-1,2-bis(3,5-dimethoxy­phen­yl)ethene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969882/
https://www.ncbi.nlm.nih.gov/pubmed/21577559
http://dx.doi.org/10.1107/S160053680903116X
work_keys_str_mv AT ritterstefanie trans12bis35dimethoxyphenylethene
AT neudorfljorgm trans12bis35dimethoxyphenylethene
AT velderjanna trans12bis35dimethoxyphenylethene
AT schmalzhansgunther trans12bis35dimethoxyphenylethene

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