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The Isolation of Episulphones from the Ramberg-Bäcklund Rearrangement; Part 3<sup>1</sup>
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1993
Year
BiologyRamberg-bäcklund RouteEngineeringNatural SciencesDiversity-oriented SynthesisMolecular BiologyAcyclic EpisulphoneOrganic ChemistryStereoselective SynthesisChemistryNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringRamberg-bäcklund RearrangementSeveral α-Halothiane 1,1-Dioxides
Information on the scope and limitations of the "Ramberg-Bäcklund" approach to episulfone synthesis is provided. Several α-halothiane 1,1-dioxides have been converted into the corresponding isolable episulphones, but attempts to extend this procedure to related α-halo-thiepane, thiolane and thietane dioxides were unsuccessful. The first example of an acyclic episulphone to be prepared by the Ramberg-Bäcklund route is described.