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Issue 12, 2012
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Wittig-olefination via an yttrium-coordinated betaine

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We report the synthesis of an yttrium phosphonium methylide complex and its reaction with benzophenone to form an excedingly rare hydrocarbon soluble metal-coordinated betaine. While this reaction models the C–C σ-bond formation step of the Wittig reaction under salt-conditions, addition of Ph3P[double bond, length as m-dash]O to the betaine complex results in formation of 1,1-diphenylethene.

Graphical abstract: Wittig-olefination via an yttrium-coordinated betaine

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The article was received on 16 Oct 2011, accepted on 29 Nov 2011 and first published on 03 Jan 2012

Article type: Communication
DOI: 10.1039/C2CC16431K
Citation: Chem. Commun., 2012,48, 1745-1747

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    Wittig-olefination via an yttrium-coordinated betaine

    M. R. Crimmin and A. J. P. White, Chem. Commun., 2012, 48, 1745
    DOI: 10.1039/C2CC16431K

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