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Virginia Tech
A study of the displacement of halogen from chlorinated heteroaromatic azines by dialkali salts of benzoylacetone, disodio salts of certain 2-hydroxy-4-methylpyrimidines, and the methylsulfinyl carbanion
Abstract
dc:description.abstractHalogenated monocyclic and bicyclic heteroaromatic azines, possessing a six or ten w-electron system and one or two ring nitrogens, have been shown to undergo nucleophilic displacement of halide ion with a variety of nucleophiles. A detailed review of the relative reactivity of compounds of these classes, as well as halogenated heteroaromatic azines containing as many as four nitrogen atoms has appeared.
Degree
thesis:*- Name thesis:degree_name
- Ph. D.
- Level thesis:degree_level
- doctoral
- Discipline thesis:degree_discipline
- Chemistry
- Department dc:contributor.department
- Chemistry
- Grantor dc:publisher
- Virginia Tech
- Year dc:date.issued
- 1971
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Greene, James Carson
- Chair dc:contributor.committeechair
-
- Wolfe, James F.
- Committee members dc:contributor.committeemember
-
- Clifford, Alan F.
- Ogliaruso, Michael A.
- Dillard, John G.
- Ward, Thomas C.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- In Copyright
- Licence dc:rights.uri
- Language dc:language.iso
- en
Identifiers
dc:identifier.*- Dc Identifier Other
- etd-08252008-162325
- OAI identifier oai:identifier
- oai:vtechworks.lib.vt.edu:10919/28796