trans-1,2-Bis(3,5-dimethoxyphenyl)ethene
The title compound, C18H20O4, 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 conformat...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2009-09-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S160053680903116X |
| _version_ | 1819278083881959424 |
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| author | Stefanie Ritter Jörg-M. Neudörfl Janna Velder Hans-Günther Schmalz |
| author_facet | Stefanie Ritter Jörg-M. Neudörfl Janna Velder Hans-Günther Schmalz |
| author_sort | Stefanie Ritter |
| collection | DOAJ |
| description | The title compound, C18H20O4, 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. |
| first_indexed | 2024-12-24T00:06:22Z |
| format | Article |
| id | doaj.art-f9eaac39aef6476c840d4e4e7158b973 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-24T00:06:22Z |
| publishDate | 2009-09-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-f9eaac39aef6476c840d4e4e7158b9732022-12-21T17:25:00ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-09-01659o2150o215010.1107/S160053680903116Xtrans-1,2-Bis(3,5-dimethoxyphenyl)etheneStefanie RitterJörg-M. NeudörflJanna VelderHans-Günther SchmalzThe title compound, C18H20O4, 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.http://scripts.iucr.org/cgi-bin/paper?S160053680903116X |
| spellingShingle | Stefanie Ritter Jörg-M. Neudörfl Janna Velder Hans-Günther Schmalz trans-1,2-Bis(3,5-dimethoxyphenyl)ethene Acta Crystallographica Section E |
| 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 |
| url | http://scripts.iucr.org/cgi-bin/paper?S160053680903116X |
| work_keys_str_mv | AT stefanieritter trans12bis35dimethoxyphenylethene AT jamp246rgmneudamp246rfl trans12bis35dimethoxyphenylethene AT jannavelder trans12bis35dimethoxyphenylethene AT hansgamp252ntherschmalz trans12bis35dimethoxyphenylethene |