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|Title:||Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition|
|Authors:||Loh, T.-P. |
|Citation:||Loh, T.-P., Wei, L.-L. (1998-06-25). Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition. Tetrahedron 54 (26) : 7615-7624. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4020(98)00394-9|
|Abstract:||In the presence of a catalytic amount of indium (III) trichloride (InCl3) (20 mol%), ketene silyl enol ethers react quickly with α, β- unsaturated ketones and esters to afford the corresponding Michael adducts in moderate to good yields. Indium(III) trichloride can be recovered and reused without decrease in yields.|
|Appears in Collections:||Staff Publications|
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