Issue 2, 2014

Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines

Abstract

Facile access to trisubstituted pyridines from α-chloro acetic ester and unsaturated imines is achieved. DMAP-catalyzed activation of ester to form an enolate intermediate constitutes a key reaction step. On the application side, the wide availability and low cost of the substrates and catalysts make this method very attractive.

Graphical abstract: Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines

Supplementary files

Article information

Article type
Research Article
Submitted
20 Nov 2013
Accepted
26 Dec 2013
First published
27 Jan 2014

Org. Chem. Front., 2014,1, 148-150

Author version available

Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines

L. Hao, X. Chen, S. Chen, K. Jiang, J. Torres and Y. R. Chi, Org. Chem. Front., 2014, 1, 148 DOI: 10.1039/C3QO00045A

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