I. Reactions of non-activated aryl halides with strong basic and nucleophilic agents. II. Evidence for cyclohexene as an intermediate in the coupling reaction of phenyllithium with 1-chlorocyclohexene. III. Reactions of non-activated aryl halides with strong bases at high temperatures. IV. The synthesis of some four-membered ring compounds
NOTE: Text or symbols not renderable in plain ASCII are indicated by [...]. Abstract is included in .pdf document. Part I. Previous studies have shown that non-activated aryl halides are aminated by alkali amides in liquid ammonia by the way of a benzyne intermediate. Nucleophilic substitution prod...
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https://thesis.library.caltech.edu/154/1/Scardiglia_f_1958.pdfScardiglia, Franco (1958) I. Reactions of non-activated aryl halides with strong basic and nucleophilic agents. II. Evidence for cyclohexene as an intermediate in the coupling reaction of phenyllithium with 1-chlorocyclohexene. III. Reactions of non-activated aryl halides with strong bases at high temperatures. IV. The synthesis of some four-membered ring compounds. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/6HT7-ZC93. https://resolver.caltech.edu/CaltechETD:etd-01132006-130643 <https://resolver.caltech.edu/CaltechETD:etd-01132006-130643>