Recent advances in transition-metal-catalyzed intermolecular carbomagnesiation and carbozincation

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Abstract

Carbomagnesiation and carbozincation reactions are efficient and direct routes to prepare complex and stereodefined organomagnesium and organozinc reagents. However, carbon-carbon unsaturated bonds are generally unreactive toward organomagnesium and organozinc reagents. Thus, transition metals were employed to accomplish the carbometalation involving wide varieties of substrates and reagents. Recent advances of transition-metal-catalyzed carbomagnesiation and carbozincation reactions are reviewed in this article. The contents are separated into five sections: carbomagnesiation and carbozincation of (1) alkynes bearing an electron-withdrawing group; (2) alkynes bearing a directing group; (3) strained cyclopropenes; (4) unactivated alkynes or alkenes; and (5) substrates that have two carbon-carbon unsaturated bonds (allenes, dienes, enynes, or diynes). © 2013 Murakami and Yorimitsu.

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Murakami, K., & Yorimitsu, H. (2013, February 11). Recent advances in transition-metal-catalyzed intermolecular carbomagnesiation and carbozincation. Beilstein Journal of Organic Chemistry. https://doi.org/10.3762/bjoc.9.34

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