Greene, James Carson2014-03-142014-03-141971-11-01etd-08252008-162325http://hdl.handle.net/10919/28796Halogenated 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.vi, 97 leavesBTDapplication/pdfenIn Copyrightnucleophilic substitution reaction mechanismsLD5655.V856 1971.G74A 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 carbanionDissertationhttp://scholar.lib.vt.edu/theses/available/etd-08252008-162325/