Palladium-Catalyzed Carbonylative Conjugate Addition of Dialkylzinc
Reagents

D. W. Custar; H. Le; J. P. Morken

doi:10.1055/s-0030-1259117

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Synfacts 2011(1): 0085-0085
DOI: 10.1055/s-0030-1259117

Metal-Mediated Synthesis

Palladium-Catalyzed Carbonylative Conjugate Addition of Dialkylzinc Reagents

Contributor(s): Paul Knochel, Andreas J. Wagner
D. W. Custar, H. Le, J. P. Morken*
Boston College, Chestnut Hill, USA

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Publikationsverlauf

Publikationsdatum:
21. Dezember 2010 (online)

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Significance

1,4-Diketones are obtained in good yields from the addition of organozinc reagents to unsaturated carbonyls in the presence of carbon monoxide. Various substituted cyclic and acyclic ketones as well as unsaturated aldehydes are suitable substrates for this reaction.