64620-59-3Relevant articles and documents
A novel enamination of β-dicarbonyl compounds catalyzed by Bi(TFA)3 immobilized on molten TBAB
Khodaei, Mohammad M.,Khosropour, Ahmad R.,Kookhazadeh, Mehdi
, p. 209 - 212 (2005)
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 results in water because of their yields and reaction times.
Enamination of β-dicarbonyl compounds with amines
Khodaei,Khosropour,Cardel
scheme or table, p. 217 - 221 (2009/04/06)
Enamination of a wide variety of primary amines was successfully described with excellent chemoselectivity in the presence of catalytic amounts of β-cyclodextrin in water under mild conditions. Aliphatic amines also reacted efficiently to produce the corresponding enaminones.
An efficient method for the enamination of 1,3-dicarbonyl compounds with ceric ammonium nitrate (CAN)
Mo, Li-Ping,Liu, Shu-Fen,Li, Wan-Zhi
, p. 879 - 884 (2008/02/11)
An efficient method for the enamination of 1,3-dicarbonyl compounds by employing ceric ammonium nitrate (CAN) as the catalyst has been described. A variety of β-amino-α,β-unsaturated ketones and esters have been synthesized in excellent yield within a short reaction time under solvent-free conditions.
