Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/47516
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dc.contributor.authorHui, Benjamin Wei Qiangen_US
dc.date.accessioned2011-12-27T08:32:08Z
dc.date.available2011-12-27T08:32:08Z
dc.date.copyright2009en_US
dc.date.issued2009
dc.identifier.urihttp://hdl.handle.net/10356/47516
dc.description108 p.en_US
dc.description.abstractOn investigating new methods towards the synthesis of azaheterocycles from organic azides, a novel orthogonal route leading to the formation of isoindole and isoquinoline derivatives was discovered and developed. a-Azido carbonyl compounds bearing a 2-alkenylaryl moiety at the cc-position were precursors to the synthesis of these useful azaheterocycles via 1,3-dipolar cycloaddition and 671-electrocyclization respectively.en_US
dc.rightsNanyang Technological Universityen_US
dc.subjectDRNTU::Scienceen_US
dc.titleOrthogonal synthesis of isoindole and isoquinoline derivatives from organic azidesen_US
dc.typeThesisen_US
dc.contributor.supervisorChiba Shunsukeen_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degree​Master of Scienceen_US
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