Reactions of organomercury fulminates with acetylene derivatives |
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Authors: | Francesco De Sarlo Antonio Guarna Andrea Goti Alberto Brandi |
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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 |
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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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