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Reactions of L-Cyanobromolycopodine

dc.contributor.advisorMacLean, D. B.
dc.contributor.authorSong, Won-Ryul
dc.contributor.departmentChemistryen_US
dc.date.accessioned2021-04-25T19:07:21Z
dc.date.available2021-04-25T19:07:21Z
dc.date.issued1958-04
dc.description.abstractThe reaction of L-cyanobromolycopodine with alkali proceeds with elimination of hydrogen bromide and a new ring is formed in the process, The properties of the compound, L-cyclocyanolycopodine, re­sulting from this cyclization reaction have been studied and a mechanism for its formation has been postulated. The olefin corresponding to that expected from the elimination of hydrogen bromide from L-cyanobromolycepodine has been prepared indirectly and the oxidative degra­dation of the olefin has boon investigated.en_US
dc.description.degreeMaster of Science (MS)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/26343
dc.language.isoenen_US
dc.subjectreactionsen_US
dc.subjectcyanobromolycopodineen_US
dc.titleReactions of L-Cyanobromolycopodineen_US
dc.typeThesisen_US

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