dc.contributor.author |
Hall, David |
en |
dc.date.accessioned |
2007-06-22T03:29:56Z |
en |
dc.date.available |
2007-06-22T03:29:56Z |
en |
dc.date.issued |
1954 |
en |
dc.identifier |
THESIS 548.3 H17c |
en |
dc.identifier.citation |
Thesis (PhD)--University of Auckland, 1954 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/524 |
en |
dc.description |
Full text is available to authenticated members of The University of Auckland only. |
en |
dc.description.abstract |
Although substituted hydroxyamidines (a) are well known, the free compounds (b) appear to be tautomerically unstable, and have been considered better described as amidoximes (c).Although substituted hydroxyamidines are well known, the free compounds appear to be tautomerically unstable, and have been considered better described as amidoxines. They possess acidic properties analagous to those of the amines and undergo numberous reactions consistent with this latter structure. |
en |
dc.language.iso |
en |
en |
dc.publisher |
ResearchSpace@Auckland |
en |
dc.relation.ispartof |
PhD Thesis - University of Auckland |
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dc.relation.isreferencedby |
UoA9921609814002091 |
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dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated |
en |
dc.rights |
Restricted Item. Available to authenticated members of The University of Auckland. |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
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dc.title |
The Crystal Structure of Formamidoxine |
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dc.type |
Thesis |
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thesis.degree.discipline |
Science |
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thesis.degree.grantor |
University of New Zealand - Auckland University College |
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thesis.degree.level |
Doctoral |
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thesis.degree.name |
PhD |
en |
dc.rights.holder |
Copyright: The author |
en |
dc.identifier.wikidata |
Q111963702 |
|