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Trans-1,2-Bis(3,5-dimethoxy-phen-yl)ethene.


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

SUBMITTER: Ritter S 

PROVIDER: S-EPMC2969882 | biostudies-other | 2009

REPOSITORIES: biostudies-other

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trans-1,2-Bis(3,5-dimethoxy-phen-yl)ethene.

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

Acta crystallographica. Section E, Structure reports online 20090815 Pt 9


The title compound, C(18)H(20)O(4), was prepared in high yield from 3,5-dimethoxy-styrene via a Ru-catalysed homo-olefin metathesis. Exclusive formation of the E-configurated isomer was observed. Inter-estingly, one symmetric unit contains two mol-ecules adopting an s-syn-anti and and an all-s-anti conformation. ...[more]

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