Fuctionalized Alkyl Quinolines: Synthesis and Characterization

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dc.contributor.authorDripps, Rachel B.
dc.creatorDripps, Rachel B.
dc.date2009-07-17
dc.date.accessioned2009-09-22T20:29:19Z
dc.date.availableNO_RESTRICTION
dc.date.available2009-09-22T20:29:19Z
dc.date.issued2009-09-22T20:29:19Z
dc.description.abstractNovel syntheses using 4-methoxy-2-methylquinoline were attempted by using a strong base to remove the most acidic proton, one of the protons of the methyl in the 2-position, to generate a carbanion. Upon the introduction of a halide with an electrophile, the electrophile will attack the carbanion where the proton was removed in an SN2 reaction to make a new compound. The methods for how this type of reaction was tried were attempted temperatures and bases are described. The DEPT-90 and 135 of 4-methoxy-2-methylquinoline were run, analyzed and the spectra are given. The DEPT spectra for this compound constitute a new contribution to the reference information for 4-methoxy-2-methylquinoline.
dc.identifier.urihttps://hdl.handle.net/1920/5613
dc.language.isoen_US
dc.subjectQuinolines
dc.subjectAlkyl quinolines
dc.subject4-methoxy-2-methylquinoline
dc.subject2-[4-(1,3)-dioxolan-2-yl)butyl]-4-methoxyquinoline
dc.titleFuctionalized Alkyl Quinolines: Synthesis and Characterization
dc.typeThesis
thesis.degree.disciplineChemistry
thesis.degree.grantorGeorge Mason University
thesis.degree.levelMaster's
thesis.degree.nameMaster of Science in Chemistry

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