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http://hdl.handle.net/11375/23667
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DC Field | Value | Language |
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dc.contributor.advisor | MacLean, David B. | - |
dc.contributor.author | Adams, Kenneth A.H. | - |
dc.date.accessioned | 2018-12-17T22:21:15Z | - |
dc.date.available | 2018-12-17T22:21:15Z | - |
dc.date.issued | 1958-09 | - |
dc.identifier.uri | http://hdl.handle.net/11375/23667 | - |
dc.description.abstract | The amino acid C14H19O4N, obtained from annotinine by oxidative fission of ring A, has been converted to the o,N-diacetyl acyclic anhydride C18H22O6N, and the anhydride ring has been shown to be five-membered. Oxidation studies have been carried out on the N-methyl lactone C17H27O2N, obtained by fission of ring A, and the oxidation products isolated and characterized. Hofmann degradation studies on the N-methyl lactone have been carried out and the products isolated from this reaction are discussed in relation to the known structure of the alkaloid. | en_US |
dc.language.iso | en | en_US |
dc.subject | chemistry | en_US |
dc.subject | annotinine | en_US |
dc.title | Studies on the Chemistry of Annotinine | 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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adams_kenneth_ah_1958sep_masters.pdf | 25.65 MB | Adobe PDF | View/Open |
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