Photochemical cyclodehydrogenation reactions / by C.P. Joshua.

Date

1967

Authors

Joshua, Chittoor Philip

Editors

Advisors

Journal Title

Journal ISSN

Volume Title

Type:

Thesis

Citation

Statement of Responsibility

Conference Name

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

Provenance

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

Description

Typescript
127 leaves, 3 reprints : ill.

Access Status

Rights

License

Grant ID

Published Version

Call number

Persistent link to this record