dc.contributor.authorJing, Zhenzhong
dc.contributor.authorLiu, Jin
dc.contributor.authorChin, Kek Foo
dc.contributor.authorChen, Wenchao
dc.contributor.authorTan, Choon-Hong
dc.contributor.authorJiang, Zhiyong
dc.identifier.citationJing, Z., Liu, J., Chin, K. F., Chen, W., Tan, C.-H., & Jiang, Z. (2014). Chiral bicyclic guanidine-catalysed conjugate addition of α-fluoro-β-ketoesters to cyclic enones. Australian journal of chemistry, 67(7), 1119-1123.en_US
dc.description.abstractBy utilising a chiral bicyclic guanidine as catalyst and triethylamine as additive, the first asymmetric Michael addition of α-fluoro-β-ketoesters to various cyclic enones has been successfully developed, affording a variety of Michael adducts with potential synthetic utilities with satisfactory stereoselectivity (up to 94 % ee and 4.3 : 1 dr).en_US
dc.format.extent11 p.en_US
dc.relation.ispartofseriesAustralian journal of chemistryen_US
dc.rights© 2014 CSIRO. This is the author created version of a work that has been peer reviewed and accepted for publication by Australian Journal of Chemistry, CSIRO. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1071/CH14187].en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry
dc.titleChiral bicyclic guanidine-catalysed conjugate addition of α-fluoro-β-ketoesters to cyclic enonesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.versionAccepted versionen_US
dc.contributor.organizationUniversity of Ministry of Educationen_US

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