Attempts Towards the Synthesis of Substituted Pyrrolines

dc.contributor.advisorDagne Ermias (PhD)
dc.contributor.authorMammo Wendimagegn
dc.date.accessioned2018-06-26T13:03:19Z
dc.date.accessioned2023-11-09T16:18:06Z
dc.date.available2018-06-26T13:03:19Z
dc.date.available2023-11-09T16:18:06Z
dc.date.issued1982-06
dc.description.abstractIn this project, the reactions of several functionalized compounds possessing the nicotine skeleton have been investigated. Studies also have been conducted on the cycloaddition reactions of C-pyridyl-h-methylnitrone with three olefinic compounds namely, allyl chloride, allyl bromide and allyl alcohol. Plausible mechanisms have been suggested for the formation of nicotine and nicotyrine by the reduction of 5-methoxycotinine and related compounds with lithium aluminum hydride. In the course of this work four new compounds, namelp 4-hydroxynicotine, 4-chloronicotine, 4-hydro:<y~l-methy1 -2-phenylpyrrolidine and 4-methoxy-l-methyl-2~phenylpyrrolidine, have been synthesized and their structures establisheden_US
dc.identifier.urihttp://etd.aau.edu.et/handle/12345678/3734
dc.language.isoenen_US
dc.publisherAddis Ababa Universtyen_US
dc.subjectSubstituted Pyrrolinesen_US
dc.titleAttempts Towards the Synthesis of Substituted Pyrrolinesen_US
dc.typeThesisen_US

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