Typescript / 127 leaves, 3 reprints : ill. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / The photochemical reactions of benzalaniline and other substituted Schiff bases in 98% sulphuric acid were examined. Benzalaniline was found to undergo photochemical cyclohydrogenation to phenanthridine and simultaneous reduction to N-benzylaniline. Substituted Schiff bases, however, did not undergo photochemical cyclization; and possible causes of the photochemical stability of these compunds are discussed. / Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 1967
| Identifer | oai:union.ndltd.org:ADTP/262146 |
| Date | January 1967 |
| Creators | Joshua, Chittoor Philip |
| Publisher | Adelaide, |
| Source Sets | Australiasian Digital Theses Program |
| Language | en_US |
| Detected Language | English |
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