Der Enolether (I) reagiert mit dem Chlormethylbutin (II) "unter Dehydrochlorierungsbedingungen zu dem Cyclopropan (III), dessen Säurekatalysierte Hydrolyse zum Dienon (IV) führt.
Die Thermolyse von α‐Diazo‐β‐dicarbonylverbindungen mit Enoläthern in Gegenwart von Cu‐Katalysatoren wie Bis‐(acetylacetonyß‐Cu (A) bzw. (CH3O)3P‐CuJ (B) wird untersucht.
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