In contrast, the novel synthesis procedure enables the production of adamantane derivatives under mild reaction conditions and at lower temperatures. The syntheses are chemo- and regioselective, so that a multitude of functional groups can be selectively introduced. The production method of amino adamantane derivatives, based on the present invention, allows for the direct introduction of amido groups without prior halogenation and therewith offers an alternative to conventional methods. Further methods, based on the present invention, allow for the direct production of 5,7-substituted 3-amino adamantane 1-carboxylic acids, as well as their linkage to oligomers. Therapeutic uses of the novel compounds: antiviral agents, GABA modulation, components of peptide catalysts, artificial ion channels.
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