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Issue 28, 2009
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Nickel-catalyzed [2 + 2 + 2] cycloaddition of arynes and an unactivated alkene: synthesis of 9,10-dihydrophenanthrene derivatives

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Abstract

A nickel-catalyzed [2 + 2 + 2] cycloaddition of two molecules of aryne and an alkene moiety in a α,ω-diene afforded 9,10-dihydrophenanthrene derivatives in good yields.

Graphical abstract: Nickel-catalyzed [2 + 2 + 2] cycloaddition of arynes and an unactivated alkene: synthesis of 9,10-dihydrophenanthrene derivatives

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Publication details

The article was received on 14 Apr 2009, accepted on 11 May 2009 and first published on 10 Jun 2009


Article type: Communication
DOI: 10.1039/B907476G
Citation: Chem. Commun., 2009, 4284-4286
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    Nickel-catalyzed [2 + 2 + 2] cycloaddition of arynes and an unactivated alkene: synthesis of 9,10-dihydrophenanthrene derivatives

    N. Saito, K. Shiotani, A. Kinbara and Y. Sato, Chem. Commun., 2009, 4284
    DOI: 10.1039/B907476G

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