Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.201000562
Title: Highly enantioselective amination reactions of fluorinated keto esters catalyzed by novel chiral guanidines derived from cinchona alkaloids
Authors: Han, X.
Zhong, F.
Lu, Y. 
Keywords: asymmetric amination
chiral guanidines
Cinchona alkaloids
fluorination substituent
organocatalysis
Issue Date: 2-Nov-2010
Citation: Han, X., Zhong, F., Lu, Y. (2010-11-02). Highly enantioselective amination reactions of fluorinated keto esters catalyzed by novel chiral guanidines derived from cinchona alkaloids. Advanced Synthesis and Catalysis 352 (16) : 2778-2782. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.201000562
Abstract: Novel Cinchona alkaloid-derived guanidines catalyze stereoselective aminations of fluorinated keto esters, affording products with fluorine-containing quaternary stereogenic centers in excellent yields and with moderate to high enantioselectivities. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title: Advanced Synthesis and Catalysis
URI: http://scholarbank.nus.edu.sg/handle/10635/76303
ISSN: 16154150
DOI: 10.1002/adsc.201000562
Appears in Collections:Staff Publications

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