Please use this identifier to cite or link to this item: https://doi.org/10.1039/b823184b
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dc.titleAsymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: Uses of fluorinated methines as nucleophiles
dc.contributor.authorHan, X.
dc.contributor.authorLuo, J.
dc.contributor.authorLiu, C.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:32:34Z
dc.date.available2014-06-23T05:32:34Z
dc.date.issued2009
dc.identifier.citationHan, 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
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75618
dc.description.abstractOrganocatalytic 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b823184b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/b823184b
dc.description.sourcetitleChemical Communications
dc.description.issue15
dc.description.page2044-2046
dc.description.codenCHCOF
dc.identifier.isiut000264675300033
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