Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/47993
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dc.contributor.authorLim, Juan Mei
dc.date.accessioned2012-02-02T06:45:04Z
dc.date.available2012-02-02T06:45:04Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.identifier.urihttp://hdl.handle.net/10356/47993
dc.description.abstractFunctionalization of enamides via allylic alkylation was achieved under the catalysis of palladium. The 5-membered N-(1H-inden-3-yl)acetamides afforded the corresponding allylic alkylation products 3 in high yields. On the other hand, the 6-membered N-(3,4- dihydronaphthalen-1-yl)acetamides besides giving 3 in moderate yields, also provided another product 3’, wherein the enamide functional group had been hydrolyzed to a ketone group.en_US
dc.format.extent39 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Scienceen_US
dc.titlePalladium-catalyzed allylic alkylation of enamides and allylic acetatesen_US
dc.typeThesis
dc.contributor.supervisorLoh Teck Pengen_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degreeMaster of Scienceen_US
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