Please use this identifier to cite or link to this item:
http://hdl.handle.net/11375/23667Full metadata record
| DC Field | Value | Language |
|---|---|---|
| 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 | |
|---|---|---|---|---|
| adams_kenneth_ah_1958sep_masters.pdf | 25.65 MB | Adobe PDF | View/Open |
Items in MacSphere are protected by copyright, with all rights reserved, unless otherwise indicated.
