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Please use this identifier to cite or link to this item: https://doi.org/10.1039/b816307c
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dc.titleAsymmetric organocatalytic Michael addition of ketones to vinyl sulfone
dc.contributor.authorZhu, Q.
dc.contributor.authorCheng, L.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:32:37Z
dc.date.available2014-06-23T05:32:37Z
dc.date.issued2008
dc.identifier.citationZhu, Q., Cheng, L., Lu, Y. (2008). Asymmetric organocatalytic Michael addition of ketones to vinyl sulfone. Chemical Communications (47) : 6315-6317. ScholarBank@NUS Repository. https://doi.org/10.1039/b816307c
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75623
dc.description.abstractHighly enantioselective organocatalytic Michael addition of ketones to vinyl sulfone catalyzed by a cinchona alkaloid-derived primary amine is reported for the first time; the described synthetic methodology was applied to the synthesis of sodium cyclamate. © The Royal Society of Chemistry 2008.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b816307c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/b816307c
dc.description.sourcetitleChemical Communications
dc.description.issue47
dc.description.page6315-6317
dc.description.codenCHCOF
dc.identifier.isiut000261742300013
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