Issue 20, 2003

An efficient and inexpensive catalyst system for the aza-Michael reactions of enones with carbamates

Abstract

A new strategy which uses very cheap FeCl3 as an effective catalyst in the presence of Me3SiCl has been developed for the conjugate addition of enones and chalcone with unactivated weakly nucleophilic carbamates.

Graphical abstract: An efficient and inexpensive catalyst system for the aza-Michael reactions of enones with carbamates

Supplementary files

Article information

Article type
Communication
Submitted
08 Jul 2003
Accepted
05 Sep 2003
First published
17 Sep 2003

Chem. Commun., 2003, 2570-2571

An efficient and inexpensive catalyst system for the aza-Michael reactions of enones with carbamates

L. Xu, C. Xia and X. Hu, Chem. Commun., 2003, 2570 DOI: 10.1039/B307733K

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