LiClO4 CATALYZED AZA-MICHAEL ADDITION OF SECONDARY AMINES TO α,β-UNSATURATED ESTERS UNDER A SOLVENT-FREE CONDITION
2018 ◽
Vol 54
(2C)
◽
pp. 537
Keyword(s):
An efficient aza-Michael addition of secondary amines to some α,β-unsaturated esters hasbeen carried out using LiCLO4 as a catalyst. β-amino esters were obtained in high yields at roomtemperature without using solvent.