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http://hdl.handle.net/11375/29868
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DC Field | Value | Language |
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dc.contributor.advisor | MacLean, D. B. | - |
dc.contributor.author | Harrison, William Ashley | - |
dc.date.accessioned | 2024-06-17T21:41:07Z | - |
dc.date.available | 2024-06-17T21:41:07Z | - |
dc.date.issued | 1957-04 | - |
dc.identifier.uri | http://hdl.handle.net/11375/29868 | - |
dc.description.abstract | The ring opened in the formation of α-cyanobromolycopodine has been found to be six-membered or larger. The product of hydrogenation of β-cyanobromolycopodine in alkaline medium has been shown to be the cyclized compound, C17H24ON2, not β-cyanolycopodine, C17H26ON2, as thought previously. A study was made of the β-cyclized compound but it could not be ascertained whether it has a ketone or an enol-ether structure. The possibility of a β-piperidone structure for lycopodine is discussed | en_US |
dc.language.iso | en | en_US |
dc.subject | lycopodine | en_US |
dc.subject | chemistry | en_US |
dc.subject | structure | en_US |
dc.subject | formation | en_US |
dc.title | Studies on the Structure of Lycopodine | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | Chemistry | en_US |
dc.description.degreetype | Thesis | en_US |
dc.description.degree | Master of Science (MS) | en_US |
Appears in Collections: | Digitized Open Access Dissertations and Theses |
Files in This Item:
File | Description | Size | Format | |
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Harrison_William_1957Apr_Masters.pdf | 2.43 MB | Adobe PDF | View/Open |
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