Issue 20, 2003
From the journal:

Chemical Communications

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

Li-Wen Xu,a   Chun-Gu Xia*a  and  Xiao-Xue Hua  

* Corresponding authors

a State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physic, Chinese Academy of Science, Lanzhou, 730000, P R China
E-mail: cgxia@ns.lzb.ac.cn
Fax: 86-931-8277088

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

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Article information

DOI
https://doi.org/10.1039/B307733K
Article type
Communication
Submitted
08 Jul 2003
Accepted
05 Sep 2003
First published
17 Sep 2003

Chem. Commun., 2003, 2570-2571

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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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