Please use this identifier to cite or link to this item:
|Title:||Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition||Authors:||Loh, T.-P.
|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|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Aug 15, 2020
WEB OF SCIENCETM
checked on Aug 7, 2020
checked on Aug 2, 2020
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.