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Please use this identifier to cite or link to this item: https://doi.org/10.1002/chem.201002202
DC FieldValue
dc.titleEnantioselective synthesis of coumarins catalyzed by a bifunctional amine-thiourea catalyst
dc.contributor.authorGao, Y.
dc.contributor.authorRen, Q.
dc.contributor.authorWang, L.
dc.contributor.authorWang, J.
dc.date.accessioned2014-06-23T05:38:42Z
dc.date.available2014-06-23T05:38:42Z
dc.date.issued2010-11-22
dc.identifier.citationGao, Y., Ren, Q., Wang, L., Wang, J. (2010-11-22). Enantioselective synthesis of coumarins catalyzed by a bifunctional amine-thiourea catalyst. Chemistry - A European Journal 16 (44) : 13068-13071. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201002202
dc.identifier.issn09476539
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76110
dc.description.abstractEfficient excess: An efficient and facile enantioselective Michael addition reaction through hydrogen-bonding catalysis for the synthesis of coumarin complexes has been developed (see scheme). A simple bifunctional amine-thiourea small molecule has been discovered to catalyze this process with high yields and high to excellent enantiomeric excesses. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/chem.201002202
dc.sourceScopus
dc.subjectasymmetric catalysis
dc.subjectcoumarins
dc.subjectMichael addition
dc.subjectorganocatalysis
dc.subjectthioureas
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/chem.201002202
dc.description.sourcetitleChemistry - A European Journal
dc.description.volume16
dc.description.issue44
dc.description.page13068-13071
dc.description.codenCEUJE
dc.identifier.isiut000285230000010
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