Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: Uses of fluorinated methines as nucleophiles

Please use this identifier to cite or link to this item: https://doi.org/10.1039/b823184b

Title:	Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: Uses of fluorinated methines as nucleophiles
Authors:	Han, X. Luo, J. Liu, C. Lu, Y.
Issue Date:	2009
Citation:	Han, X., Luo, J., Liu, C., Lu, Y. (2009). Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: Uses of fluorinated methines as nucleophiles. Chemical Communications (15) : 2044-2046. ScholarBank@NUS Repository. https://doi.org/10.1039/b823184b
Abstract:	Organocatalytic asymmetric Michael reactions of fluorinated nucleophiles with nitroolefins catalyzed by Cinchona alkaloid-derived thiourea catalysts generated the desired Michael products containing vicinal fluorinated quaternary and tertiary chiral centers with exceptional enantioselectivity. © 2009 The Royal Society of Chemistry.
Source Title:	Chemical Communications
URI:	http://scholarbank.nus.edu.sg/handle/10635/75618
ISSN:	13597345
DOI:	10.1039/b823184b
Appears in Collections:	Staff Publications

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