Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/32269
Title: Water-compatible iminium activation : highly enantioselective organocatalytic michael addition malonates to alpha,beta-unsaturated enones
Authors: Mao, Z
Jia, Y
Li, W
Wang, R
Issue Date: 2010
Publisher: American Chemical Society
Source: Journal of organic chemistry, 2010, v. 75, no. 21, p. 7428-7430 How to cite?
Journal: Journal of organic chemistry 
Abstract: The highly enantioselective Michael addition of malonates to alpha,beta-unsaturated ketones in water was reported to be catalyzed by a primary secondary diamine catalyst containing a long alkyl chain. This asymmetric Michael addition process was found to be effective for a variety of alpha,beta-unsaturated ketones.
URI: http://hdl.handle.net/10397/32269
ISSN: 0022-3263
EISSN: 1520-6904
DOI: 10.1021/jo101188m
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