Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/39870
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dc.contributor.authorGao, Zhi Ming.-
dc.date.accessioned2010-06-07T06:33:28Z-
dc.date.available2010-06-07T06:33:28Z-
dc.date.copyright2010en_US
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/10356/39870-
dc.description.abstractIn this research report, Fe(III)- and Au(I)-catalyzed cyclizations of arene-alkynes were investigated. Au(I) catalyst has shown to be of very efficient catalytic activity for intramolecular hydroarylations of arene-alkynes with promising yields at mild conditions whether the alkyne is substituted by electron-withdrawing or electron-donating group. While Fe(III) was shown to be sensitive to the substitute on the alkyne moiety, electron-withdrawing group substituted alkynes did not proceed to cyclized products, but for the electron-donating group substituted arene-alkynes, Fe(III) catalyst showed as high efficiency as Au(I) catalyst.en_US
dc.format.extent51 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Heterocyclic compoundsen_US
dc.titleFe(III)- and Au(I)-catalyzed cyclization of arene-alkynes.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degreeBachelor of Science in Chemistry and Biological Chemistryen_US
dc.contributor.supervisor2Sunggak Kimen_US
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Appears in Collections:SPMS Student Reports (FYP/IA/PA/PI)
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