Reaction of tetracarbonyl(Ο-allyl)mangan
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William S. Vaughan; Henry H. Gu; Keith F. McDaniel
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Article
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1997
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Elsevier Science
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French
β 192 KB
## Nucleophilic attack an tetracarbonyl(~aUyl)manganese takes place at the terminus of the ~.system, generating aUylated products in 44-95% yield after oxidation. Stabilized nucleophiles (pKa 12-20) give mainly his aUylation whereas nonstabilized nucleophiles (pKa [25][26][27][28][29][30][31][32][