[2,3]-Sigmatropic Rearrangement of Allylic Selenimides: Strategy for the Synthesis of Peptides, Peptidomimetics, and N-Aryl Vinyl Glycines
Author:
Affiliation:
1. Department of Chemistry, Imperial College London, South Kensington, London SW7 2AZ, U.K.
2. GSK Stevenage, Gunnels Wood Road, Stevenage Herts SG1 2NY, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo500341e
Reference49 articles.
1. Peptidomimetics – A Versatile Route to Biologically Active Compounds
2. Peptidomimetics—Tailored Enzyme Inhibitors
3. 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/
4. Oxaziridine-Mediated Amination of Branched Allylic Sulfides: Stereospecific Formation of Allylic Amine Derivatives via [2,3]-Sigmatropic Rearrangement
5. Exploiting Organocatalysis: Enantioselective Synthesis of Vinyl Glycines by Allylic Sulfimide [2,3] Sigmatropic Rearrangement
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