Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/40106
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dc.contributor.authorKoh, Chii Boon.-
dc.date.accessioned2010-06-10T06:25:50Z-
dc.date.available2010-06-10T06:25:50Z-
dc.date.copyright2010en_US
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/10356/40106-
dc.description.abstractA concise, asymmetric synthesis of substituted 3-pyrrolines from the corresponding amino-homoallylic alcohols derived from amino acids is described. The key step is an intramolecular hydroamination reaction catalyzed by copper(II) triflate. The 3-pyrroline products were obtained in moderate to good yields and with excellent diastereoselectivity and enantioselectivity.en_US
dc.format.extent48 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistryen_US
dc.titleSynthesis of substituted pyrrolo- and indolo-quinoxalines via the gold(i)-catalyzed tandem hydroamination-hydroarylation of pyrrole- and indole-substituted anilines with aromatic terminal alkynes.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.supervisorPhilip Wai Hong Chanen_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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