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Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201102796
DC FieldValue
dc.titleFrom the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: Asymmetric synthesis of 3(2H)-furanones
dc.contributor.authorDou, X.
dc.contributor.authorHan, X.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:40:06Z
dc.date.available2014-06-23T05:40:06Z
dc.date.issued2012-01-02
dc.identifier.citationDou, X., Han, X., Lu, Y. (2012-01-02). From the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: Asymmetric synthesis of 3(2H)-furanones. Chemistry - A European Journal 18 (1) : 85-89. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201102796
dc.identifier.issn09476539
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76224
dc.description.abstractIt all adds up! A modified Feist-Bénary reaction employing a domino Michael-alkylation sequence was designed for the enantioselective synthesis of 3(2H)-furanones. L-Threonine-derived tertiary amine/thiourea catalysts were prepared for the first time; such catalysts promoted the designed domino Michael-alkylation reactions in a highly enantioselective manner (see scheme). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/chem.201102796
dc.sourceScopus
dc.subjectasymmetric synthesis
dc.subjectdomino reactions
dc.subjectFeist-Bénary reaction
dc.subjectfuranones
dc.subjectorganocatalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/chem.201102796
dc.description.sourcetitleChemistry - A European Journal
dc.description.volume18
dc.description.issue1
dc.description.page85-89
dc.description.codenCEUJE
dc.identifier.isiut000298547800012
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