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Fuctionalized Alkyl Quinolines: Synthesis and Characterization

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dc.contributor.author Dripps, Rachel B.
dc.creator Dripps, Rachel B.
dc.date 2009-07-17
dc.date.accessioned 2009-09-22T20:29:19Z
dc.date.available NO_RESTRICTION en_US
dc.date.available 2009-09-22T20:29:19Z
dc.date.issued 2009-09-22T20:29:19Z
dc.identifier.uri https://hdl.handle.net/1920/5613
dc.description.abstract Novel 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.language.iso en_US en_US
dc.subject quinolines en_US
dc.subject alkyl quinolines en_US
dc.subject 4-methoxy-2-methylquinoline en_US
dc.subject 2-[4-(1,3)-dioxolan-2-yl)butyl]-4-methoxyquinoline en_US
dc.title Fuctionalized Alkyl Quinolines: Synthesis and Characterization en_US
dc.type Thesis en
thesis.degree.name Master of Science in Chemistry en_US
thesis.degree.level Master's en
thesis.degree.discipline Chemistry en
thesis.degree.grantor George Mason University en


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