Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79664
Title: Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines
Authors: Chi, Robin Yonggui
Hao, Lin
Chen, Xingkuan
Chen, Shaojin
Jiang, Ke
Torres, Jaume
Keywords: DRNTU::Science::Biological sciences
Issue Date: 2014
Source: Hao, L., Chen, X., Chen, S., Jiang, K., Torres, J., & Chi, Y. R. (2014). Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines. Organic chemistry frontiers, 1(2), 148-150.
Series/Report no.: Organic chemistry frontiers
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.
URI: https://hdl.handle.net/10356/79664
http://hdl.handle.net/10220/23927
DOI: 10.1039/C3QO00045A
Schools: School of Physical and Mathematical Sciences 
School of Biological Sciences 
Rights: © 2014 the Partner Organisations.
Fulltext Permission: open
Fulltext Availability: With Fulltext
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