Liebigs Annalen der Chemie

Neue Synthesemethoden, 10. β??Ketosulfone als Ethylencarbanionen??Äquivalente: die Synthese ungesättigter Carbonsäuren

D Scholz

Index: Scholz, Dieter Liebigs Annalen der Chemie, 1984 , # 2 p. 264 - 272

Full Text: HTML

Citation Number: 7

Abstract

Abstract α-Alkylthiolierte Cycloalkanone werden nach Oxidation zu Sulfonen unter Halogenierung zu α-Halogensulfonen ringgeöffnet. Ramberg-Bäcklund-Umlagerung ergibt ungesättigte Carbonsäuren, wobei die Lage der neuen Doppelbindung durch die Ringgröße der Ausgangscycloalkanone bestimmt wird.

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