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2002 amination, N-alkylation, N-arylation amination, N-alkylation, N-arylation O 0268 34 - 063 Efficient Amination of Sulfides with a Ketomalonate-Derived Ox- aziridine: Application to [2,3]-Sigmatropic Rearrangements of Allylic Sulfimides. The novel oxaziridine (III) effects efficient amination of sulfides (IV) to sulfimides (V). The reagent is applied to the [2,3]-sigmatropic rearrangement of allylic sulfimides. — (ARMSTRONG, ALAN; COOKE, RICHARD S.; Chem. Commun. (Cambridge) (2002) 8, 904-905; Dep. Chem., Imp. Coll. Sci. Technol. Med., London SW7 2AY, UK; EN) 1

ChemInform Abstract: Efficient Amination of Sulfides with a Ketomalonate-Derived Oxaziridine: Application to [2,3]-Sigmatropic Rearrangements of Allylic Sulfimides

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2002 amination, N-alkylation, N-arylation

amination, N-alkylation, N-arylationO 0268

34 - 063Efficient Amination of Sulfides with a Ketomalonate-Derived Ox-aziridine: Application to [2,3]-Sigmatropic Rearrangements of AllylicSulfimides. — The novel oxaziridine (III) effects efficient amination ofsulfides (IV) to sulfimides (V). The reagent is applied to the [2,3]-sigmatropicrearrangement of allylic sulfimides. — (ARMSTRONG, ALAN; COOKE,RICHARD S.; Chem. Commun. (Cambridge) (2002) 8, 904-905; Dep. Chem.,Imp. Coll. Sci. Technol. Med., London SW7 2AY, UK; EN)

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