Conjugate additions to α,β-unsaturated carbonyl compounds in aqueous media

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Abstract

Alkyl halides in the presence of zinc copper couple add smoothly to α-enones and α-enals in aqueous solvents. Sonication enhances the efficiency of the process, which leads to the conjugate adducts in high yields. The reaction follows most probably a radical pathway, and can be used for the addition of functionalized groups. © 1986.

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Petrier, C., Dupuy, C., & Luche, J. L. (1986). Conjugate additions to α,β-unsaturated carbonyl compounds in aqueous media. Tetrahedron Letters, 27(27), 3149–3152. https://doi.org/10.1016/S0040-4039(00)84739-5

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