Efficient amination of sulfides with a ketomalonate-derived oxaziridine: application to [2,3]-sigmatropic rearrangements of allylic sulfimidesElectronic supplementary information (ESI) available: experimental details and characterisation data. See http://www.rsc.org/suppdata/cc/b2/b201791a/
Chemical Communications2002Iss. 8, pp. 904–905
Citations Over TimeTop 17% of 2002 papers
Abstract
A novel N-Boc-oxaziridine is reported, derived from diethyl ketomalonate, which effects efficient amination of sulfides to sulfimides. The reagent is applied to the [2,3]-sigmatropic rearrangement of allylic sulfimides.
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