Oxaziridine-Mediated Amination of Branched Allylic Sulfides: Stereospecific Formation of Allylic Amine Derivatives via [2,3]-Sigmatropic Rearrangement
Author:
Affiliation:
1. Department of Chemistry, Imperial College London, South Kensington, London SW7 2AZ, U.K., and Organon Newhouse, Lanarkshire ML1 5SH, Scotland a.armstrong@imperial.ac.uk
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo060369s
Reference15 articles.
1. 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/
2. Amination and [2,3]-sigmatropic rearrangement of propargylic sulfides using a ketomalonate-derived oxaziridine: synthesis of N-allenylsulfenimides
3. Oxaziridine-Mediated Amination of Primary Amines: Scope and Application to a One-Pot Pyrazole Synthesis
4. Sulfimides (Sulfilimines): Applications in Stereoselective Synthesis
5. Electrophilic amination of carbanions
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