Improved Synthesis of MediPhos Ligands and Their Use in the Pd‐Catalyzed Enantioselective N‐Allylation of Glycine Esters
Author:
Affiliation:
1. Department of Chemistry University of Cologne Greinstrasse 4 50939 Koeln Germany
Funder
Universität zu Köln
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100748
Reference54 articles.
1. The Tsuji–Trost Reaction and Related Carbon–Carbon Bond Formation Reactions: Overview of the Palladium–Catalyzed Carbon–Corbon Bond Formation viaπ-Allylpalladium and Propargylpalladium Intermediates
2. For selected reviews see:
3. Asymmetric Transition Metal-Catalyzed Allylic Alkylations
4. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
5. Pd-Catalyzed Enantioselective Allylic Substitution: New Strategic Options for the Total Synthesis of Natural Products
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2. Efficient Solution Phase Synthesis of PPII Helix Mimicking Ena/VASP EVH1 Inhibitors from Proline‐Derived Modules (ProMs);European Journal of Organic Chemistry;2023-09-18
3. On the Asymmetric Iridium‐Catalyzed N‐Allylation of Amino Acid Esters: Improved Selectivities through Structural Variation of the Chiral Phosphoramidite Ligand;European Journal of Organic Chemistry;2022-03-23
4. Improved Synthesis of MediPhos Ligands and Their Use in the Pd‐Catalyzed Enantioselective N‐Allylation of Glycine Esters;European Journal of Organic Chemistry;2021-08-06
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