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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

Halogenated 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. / Ph. D.

Identiferoai:union.ndltd.org:VTETD/oai:vtechworks.lib.vt.edu:10919/28796
Date25 August 2008
CreatorsGreene, James Carson
ContributorsChemistry, Wolfe, James F., Clifford, Alan F., Ogliaruso, Michael A., Dillard, John G., Ward, Thomas C.
PublisherVirginia Tech
Source SetsVirginia Tech Theses and Dissertation
LanguageEnglish
Detected LanguageEnglish
TypeDissertation, Text
Formatvi, 97 leaves, BTD, application/pdf, application/pdf
RightsIn Copyright, http://rightsstatements.org/vocab/InC/1.0/
RelationOCLC# 34220414, LD5655.V856_1971.G74.pdf

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