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Synthesis
DOI: 10.1055/a-2646-8445
DOI: 10.1055/a-2646-8445
paper
Chiral Ligands with 1,10-Phenanthroline Scaffolds for Copper-Catalyzed Enantioselective C(sp3)−H Bond Amidation
Gefördert durch: Key R&D Program of China 2021YFA1500200
Gefördert durch: National Natural Science Foundation of China 22221002,22301145,92256301
Gefördert durch: New Cornerstone Science Foundation
Gefördert durch: Haihe Laboratory of Sustainable Chemical Transformations
We thank the National Key R&D Program of China (2021YFA1500200), National Natural Science Foundation of China (22301145, 22221002, 92256301), Haihe Laboratory of Sustainable Chemical Transformations, Fundamental Research Funds for the Central Universities, and New Cornerstone Science Foundation through the XPLORER PRIZE for financial support.

Abstract
We herein report newly developed C₂-symmetric 2,9-diarylphenanthroline ligands with easily modified chiral amide motifs, which enable Cu-catalyzed intramolecular C(sp³)–H amidation of mesylcarbamates to deliver 2-oxazolidone derivatives with up to 88:12 er.
Keywords
Chiral 1,10-phenanthroline - Copper catalysis - Nitrene C–H insertion - Carbamate ester - β-Amino alcoholsPublikationsverlauf
Eingereicht: 20. Mai 2025
Angenommen nach Revision: 01. Juli 2025
Accepted Manuscript online:
01. Juli 2025
Artikel online veröffentlicht:
22. Juli 2025
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