Israel Journal of Chemistry

Studies of the Ramberg??Bäcklund Rearrangement. Part I. Rearrangement of α??Bromo?螃漫?Keto??and α??Bromo?螃窿?Carbethoxy??Sulphones

I Shahak, ED Bergmann

文献索引：Shahak,I.; Bergmann,E.D. Israel Journal of Chemistry, 1970 , vol. 8, p. 589 - 593

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被引用次数: 2

摘要

Abstract α-Bromosulphones, carrying negative substituents (keto or carbethoxy-groups) next to the bromine atom, undergo the Ramberg-Bäcklund rearrangement and give α, β- unsaturated ketones and esters. β-Disulphones are converted into α, β-unsaturated sulphones under these conditions.