The 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. / Thesis / Master of Science (MS)
| Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/26343 |
| Date | 04 1900 |
| Creators | Song, Won-Ryul |
| Contributors | MacLean, D. B., Chemistry |
| Source Sets | McMaster University |
| Language | English |
| Detected Language | English |
| Type | Thesis |
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