Sulfoximines with α ‐Ketoester Functionalities at Nitrogen from Cyanoacetates and Air
Author:
Affiliation:
1. Institute of Organic Chemistry RWTH Aachen University Landoltweg 1 D-52074 Aachen Germany
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202001264
Reference62 articles.
1. For selected reviews on (hypervalent) iodine reagents see:
2. Hypervalent Iodine-Catalyzed Oxidative Functionalizations Including Stereoselective Reactions
3. Stoichiometric and catalytic oxidations with hypervalent organo-λ3-iodanes
4. Catalysis with In Situ-Generated (Hypo)iodite Ions for Oxidative Coupling Reactions
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3. Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones;Chemistry – A European Journal;2022-03-14
4. Lewis acid triggered N-alkylation of sulfoximines through nucleophilic ring-opening of donor–acceptor cyclopropanes: synthesis of γ-sulfoximino malonic diesters;Organic & Biomolecular Chemistry;2022
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