Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.200700326
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dc.titleChiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
dc.contributor.authorYe, W.
dc.contributor.authorJiang, Z.
dc.contributor.authorZhao, Y.
dc.contributor.authorGoh, S.L.M.
dc.contributor.authorLeow, D.
dc.contributor.authorSoh, Y.-T.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:34:08Z
dc.date.available2014-06-23T05:34:08Z
dc.date.issued2007-11
dc.identifier.citationYe, W., Jiang, Z., Zhao, Y., Goh, S.L.M., Leow, D., Soh, Y.-T., Tan, C.-H. (2007-11). Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters. Advanced Synthesis and Catalysis 349 (16) : 2454-2458. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.200700326
dc.identifier.issn16154150
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75744
dc.description.abstractA chiral bicyclic guanidine was developed as a versatile Brønsted base catalyst for the enantioselective Michael reactions of dithiomalonates and β-keto thioesters using a range of acceptors including maleimides, cyclic enones, furanone and acyclic 1,4-dicarbonylbutenes. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/adsc.200700326
dc.sourceScopus
dc.subjectAsymmetric catalysis
dc.subjectDithiomalonates
dc.subjectGuanidines
dc.subjectMichael addition
dc.subjectOrganic catalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/adsc.200700326
dc.description.sourcetitleAdvanced Synthesis and Catalysis
dc.description.volume349
dc.description.issue16
dc.description.page2454-2458
dc.description.codenJPCHF
dc.identifier.isiut000251437600008
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