Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/39938
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dc.contributor.authorWang, Stephanie Qiu Mei.-
dc.date.accessioned2010-06-08T03:49:47Z-
dc.date.available2010-06-08T03:49:47Z-
dc.date.copyright2010en_US
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/10356/39938-
dc.description.abstractNaphthalene derivatives have been found in many pharmaceuticals and luminescent materials. Herein, we report a tandem Michael Addition/Cyclisation utilizing aminocatalysis and Lewis acid catalysis to synthesize useful naphthalene derivatives under mild conditions. The Michael addition can work for a range of aldehyes, including aromatic and aliphatic ones.en_US
dc.format.extent58 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organic synthesisen_US
dc.titleSequential michael addition/cyclisation : synthesis of multi-substituted naphthalenes.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorZhong Guofuen_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degreeBachelor of Science in Chemistry and Biological Chemistryen_US
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Appears in Collections:SPMS Student Reports (FYP/IA/PA/PI)
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