Abstract
1. A comparative investigation was made of two methods for the synthesis of organomercury compounds — the diazoaliphatic method and the oxidation of hydrazone complexes of mercuric halides with mercuric oxide — for the case of 2,3-bornanedione and benzil derivatives. 2. In the case of 2,3-bornanedione both methods lead to the formation of the same types of organomercury compound in approximately the same yields. 3. In the case of benzil the method of synthesizing organomercury compounds by the oxidation of complexes formed by the monohydrazone with mercuric halides is inapplicable.
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Schedule a callMore From: Bulletin of the Academy of Sciences, USSR Division of Chemical Science
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