Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24681
Title: Uncatalyzed, green aza-Michael addition of amines to dimethyl maleate
Authors: Bosica, Giovanna
Debono, Anthony John
Keywords: Catalyst poisoning
Solvent wastes
Solvents
Aza compounds
Issue Date: 2014
Publisher: Pergamon Press
Citation: Bosica, G., & Debono, A. J. (2014). Uncatalyzed, green aza-Michael addition of amines to dimethyl maleate. Tetrahedron, 70(37), 6607-6612.
Abstract: Dimethyl maleate was found to be a very reactive and selective acceptor for the aza-Michael addition in comparison to other commonly used electron-deficient alkenes. It reacts efficiently with a variety of aliphatic amines in complete absence of any catalyst and solvent at room temperature. Under these environmentally-friendly conditions, high yields of selectively mono-adducts were obtained within short reaction times.
URI: https://www.um.edu.mt/library/oar//handle/123456789/24681
Appears in Collections:Scholarly Works - FacSciChe

Files in This Item:
File Description SizeFormat 
1-s2.0-S0040402014009983-main.pdf
  Restricted Access
563.87 kBAdobe PDFView/Open Request a copy


Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.