Type of Document	Dissertation
Author	Greene, James Carson
URN	etd-08252008-162325
Title	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
Degree	PhD
Department	Chemistry
Advisory Committee	Advisor Name Title Wolfe, James F. Committee Chair Clifford, Alan F. Committee Member Dillard, John G. Committee Member Ogliaruso, Michael A. Committee Member Ward, Thomas C. Committee Member
Keywords	nucleophilic substitution reaction mechanisms
Date of Defense	1971-11-01
Availability	unrestricted
Abstract 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.
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