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Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201202504
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dc.titleA highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction
dc.contributor.authorDou, X.
dc.contributor.authorZhong, F.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-10-16T08:18:34Z
dc.date.available2014-10-16T08:18:34Z
dc.date.issued2012-10-29
dc.identifier.citationDou, X., Zhong, F., Lu, Y. (2012-10-29). A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction. Chemistry - A European Journal 18 (44) : 13945-13948. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201202504
dc.identifier.issn09476539
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/92945
dc.description.abstractOrganocatalysis: A modified Feist-Bénary reaction employing acyclic β-ketoesters as the dinucleophile and (E)-β,β-bromo nitrostyrenes as the dielectrophile was developed for the asymmetric synthesis of 2,3-dihydrofurans. L-Threonine-derived tertiary amine/thiourea catalysts were found to be the most efficient catalysts, inducing the reaction in a highly enantioselective manner (see scheme; TBDPS=tert-butyldiphenylsilyl). 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.201202504
dc.sourceScopus
dc.subjectasymmetric synthesis
dc.subjectdomino reaction
dc.subjectFeist-Bénary reaction
dc.subjectorganocatalysis
dc.subjectsynthetic methods
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/chem.201202504
dc.description.sourcetitleChemistry - A European Journal
dc.description.volume18
dc.description.issue44
dc.description.page13945-13948
dc.description.codenCEUJE
dc.identifier.isiut000310473900004
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