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Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.201000562
DC FieldValue
dc.titleHighly enantioselective amination reactions of fluorinated keto esters catalyzed by novel chiral guanidines derived from cinchona alkaloids
dc.contributor.authorHan, X.
dc.contributor.authorZhong, F.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:41:07Z
dc.date.available2014-06-23T05:41:07Z
dc.date.issued2010-11-02
dc.identifier.citationHan, 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
dc.identifier.issn16154150
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76303
dc.description.abstractNovel 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/adsc.201000562
dc.sourceScopus
dc.subjectasymmetric amination
dc.subjectchiral guanidines
dc.subjectCinchona alkaloids
dc.subjectfluorination substituent
dc.subjectorganocatalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/adsc.201000562
dc.description.sourcetitleAdvanced Synthesis and Catalysis
dc.description.volume352
dc.description.issue16
dc.description.page2778-2782
dc.description.codenJPCHF
dc.identifier.isiut000284004200011
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