Issue 6, 2018

Nickel-catalyzed cross-coupling of β-carbonyl alkenyl pivalates with arylzinc chlorides

Abstract

The nickel-catalyzed cross-coupling reaction of β-carbonyl alkenyl pivalates with arylzinc reagents generates 3-aryl-substituted α,β-unsaturated carbonyl compounds via C–O bond cleavage. The reaction features mild reaction conditions, a wide scope of substrates, and good functional group tolerance.

Graphical abstract: Nickel-catalyzed cross-coupling of β-carbonyl alkenyl pivalates with arylzinc chlorides

Supplementary files

Article information

Article type
Paper
Submitted
29 Nov 2017
Accepted
08 Jan 2018
First published
08 Jan 2018

Org. Biomol. Chem., 2018,16, 1029-1036

Nickel-catalyzed cross-coupling of β-carbonyl alkenyl pivalates with arylzinc chlorides

W. Pan and Z. Wang, Org. Biomol. Chem., 2018, 16, 1029 DOI: 10.1039/C7OB02947K

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