A novel enamination of β-dicarbonyl compounds catalyzed by Bi(TFA)<sub>3</sub> immobilized on molten TBAB
作者:Mohammad M Khodaei、Ahmad R Khosropour、Mehdi Kookhazadeh
DOI:10.1139/v05-021
日期:2005.3.1
Enamination of a wide variety of primary amines was successfully carried out in the presence of catalytic amounts of bismuth(III) trifluoroacetate immobilized on molten tetrabutylammonium bromide as "green" media under mild conditions. This new system of the catalyst is recyclable and reusable. Generally, the results of the reaction in tetrabutylammonium bromide is better than the previously obtained
Cerium(III) Chloride Heptahydrate (CeCl3 · 7H2O) as an Efficient Enamination Catalyst in Aqueous Media
作者:M. M. Khodaei、A. R. Khosropour、M. Kookhazadeh
DOI:10.1007/s11178-005-0363-z
日期:2005.10
Cerium(III) chloride heptahydrate CeCl3 · H2O catalyzes enamination of β-dicarbonyl compounds with primary amines in aqueous medium at room temperature to afford the corresponding β-enamino ketones with high chemoselectivity.
Enamination of a wide various primary amines was successfully carried out in the presence of catalytic amounts of cerium chloride heptahydrate in ionic liquid and solvent-free conditions as 'green' media under mild reaction conditions.
A mild, efficient and environmentally friendly method for the regio- and chemoselective synthesis of enaminones using Bi(TFA)3 as a reusable catalyst in aqueous media
作者:Ahmad R. Khosropour、Mohammad M. Khodaei、Mehdi Kookhazadeh
DOI:10.1016/j.tetlet.2003.12.093
日期:2004.2
Bismuth(III) trifluoroacetate has been found to be an extremely efficient catalyst for the preparation of beta-enaminones in water. In addition, by employing this catalyst, high regio- and chemoselective enamination of carbonyl compounds was achieved. (C) 2004 Elsevier Ltd. All rights reserved.
Enamination of β-Dicarbonyl Compounds with Amines
作者:M. M. Khodaei、A. R. Khosropour、C. Cardel
DOI:10.1002/jccs.200800032
日期:2008.2
Enamination of a wide variety of primary amines was successfully described with excellent chemo-selectivity in the presence of catalytic amounts of β-cyclodextrin in water under mild conditions. Aliphatic amines also reacted efficiently to produce the corresponding enaminones.