ChemInform Abstract: Sulfoxide Induced Sigmatropic Rearrangement (SISR) of Methyl 1- Methylsulfanylvinyl Sulfoxides.
β Scribed by B. F. BONINI; M. C. FRANCHINI; G. MAZZANTI; J.-W. SLIEF; M. A. WEGMAN; B. ZWANENBURG
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Sulfoxide Induced Sigmatropic Rearrangement (SISR) of Methyl 1-Methylsulfanylvinyl Sulfoxides.
-Thiophenoxide is established as thiophilic reagent as well as base for the sequential prototropic shifts and sigmatropic rearrangement reactions of sulfoxides (I). For the SISR reaction, the conditions for the "sulfoxide piperidine and carbonyl" reactions are tried for substrate (Ia). -(BONINI, B.
π SIMILAR VOLUMES
Thermal Rearrangement of 1,3-Thiazolidine Sulfoxides: Thiosulfinate and Thioaldehyde Intermediates. -As an extension of studies on the reactivity and synthetic uses of sulfoxides and sulfenic acids, the thermal rearrangement of title compound (I) is investigated. The formation of the products (II)-
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