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Trans-Ethyl-enedi-p-phenyl-ene diacetate.


ABSTRACT: The centrosymmetric title compound, C(18)H(26)O(4), was prepared in high yield from 4-acetoxy-styrene via Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. In the crystal, a strong C-H?? inter-molecular inter-action links the mol-ecules together.

SUBMITTER: Ritter S 

PROVIDER: S-EPMC2970084 | biostudies-other | 2009

REPOSITORIES: biostudies-other

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trans-Ethyl-enedi-p-phenyl-ene diacetate.

Ritter Stefanie S   Neudörfl Jörg-M JM   Velder Janna J   Schmalz Hans-Günther HG  

Acta crystallographica. Section E, Structure reports online 20090826 Pt 9


The centrosymmetric title compound, C(18)H(26)O(4), was prepared in high yield from 4-acetoxy-styrene via Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. In the crystal, a strong C-H⋯π inter-molecular inter-action links the mol-ecules together. ...[more]

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