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Reactions of organomercury fulminates with acetylene derivatives
Authors:Francesco De Sarlo  Antonio Guarna  Andrea Goti  Alberto Brandi
Institution:Centro di studio sulla chimica e la struttura dei composti eterociclici e loro applicazione, C.N.R., Istituto di Chimica organica, Università di Firenze, via G. Capponi, 9, 50121 Firenze Italy
Abstract:Organomercury fulminates react with acetylene derivatives to give unstable 3-(organomercurio)isoxazoles, which isomerize to 2-cyanoenolates. These are hydrolyzed with hydrochloric acid to the corresponding enols and are cleaved by water at the double bond. With monosubstituted acetylenes, substitution at the free position by the organomercury residue is predominant.
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