scholarly journals LiClO4 CATALYZED AZA-MICHAEL ADDITION OF SECONDARY AMINES TO α,β-UNSATURATED ESTERS UNDER A SOLVENT-FREE CONDITION

2018 ◽  
Vol 54 (2C) ◽  
pp. 537
Author(s):  
Dau Xuan Duc

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.

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Firouzeh Nemati ◽  
Azam Beyzai

A novel one-pot synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-ones by condensation of a variety of aldehydes withβ-naphthol and urea or thiourea in the presence of wet cyanuric chloride under solvent-free condition has been described. High yields, simple procedure, easy workup, short reaction times, and avoiding the use of organic solvent are the advantages of this green methodology.


2016 ◽  
Vol 19 (1) ◽  
pp. 5-10
Author(s):  
Dung Duc Pham ◽  
Huyen Ngoc Chau ◽  
Thach Ngoc Le

KF supported on montmorillonite K10 catalyzed three-component cyclocondensation of aromatic aldehyde, cyclohexan-1,3-dione and malononitrile under ultrasound irradiation and solvent-free condition to give the corresponding 4H-pyrans in high yields. This method provides several advantages such as short time, mild condition and the catalyst can be recycled easily.


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