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dc.contributor.advisorMichael, Forrest Men_US
dc.contributor.authorPierson, Justin Michaelen_US
dc.date.accessioned2013-02-25T17:49:16Z
dc.date.available2013-02-25T17:49:16Z
dc.date.issued2013-02-25
dc.date.submitted2012en_US
dc.identifier.otherPierson_washington_0250O_10939.pdfen_US
dc.identifier.urihttp://hdl.handle.net/1773/21745
dc.descriptionThesis (Master's)--University of Washington, 2012en_US
dc.description.abstractA highly regioselective palladium catalyzed intramolecular hydroamination of substituted 1,3-dienes was achieved to create diverse nitrogen containing heterocycles. Hydroamination of 1,3-dienes goes in high yields, is selective for 1,2 addition and is suitable for a wide variety of nitrogen protect-ing groups. Insight to the mechanism of 1,3-diene hydroamination was accomplished by isolating a crucial palladium allyl complex.en_US
dc.format.mimetypeapplication/pdfen_US
dc.language.isoen_USen_US
dc.rightsCopyright is held by the individual authors.en_US
dc.subjectdiene; Hydroamination; Intramolecular; Palladiumen_US
dc.subject.otherChemistryen_US
dc.subject.otherChemistryen_US
dc.titlePalladium(II) Catalyzed Intramolecular Hydroamination of 1,3-dienesen_US
dc.typeThesisen_US
dc.embargo.termsNo embargoen_US


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