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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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