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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 |
| Appears in Collections: | Staff Publications |
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