Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4020(98)00394-9
Title: Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition
Authors: Loh, T.-P. 
Wei, L.-L.
Keywords: Indium trichloride
Michael reaction
Neat condition
Issue Date: 25-Jun-1998
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.
Source Title: Tetrahedron
URI: http://scholarbank.nus.edu.sg/handle/10635/94041
ISSN: 00404020
DOI: 10.1016/S0040-4020(98)00394-9
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