Photochemical cyclodehydrogenation reactions / by C.P. Joshua.
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Date
1967
Authors
Joshua, Chittoor Philip
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Thesis
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Abstract
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.
School/Discipline
Dept. of Organic Chemistry
Dissertation Note
Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 1967
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Copyright material removed from digital thesis. See print copy in University of Adelaide Library for full text.
This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
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127 leaves, 3 reprints : ill.
127 leaves, 3 reprints : ill.