Synthesis
DOI: 10.1055/a-2646-8445
paper

Chiral Ligands with 1,10-Phenanthroline Scaffolds for Copper-Catalyzed Enantioselective C(sp3)−H Bond Amidation

1   College of Chemistry, Nankai University, Tianjin, China
,
Xiao-Yu Li
1   College of Chemistry, Nankai University, Tianjin, China
,
Wen Che
1   College of Chemistry, Nankai University, Tianjin, China
,
Hao-Rui Sang
1   College of Chemistry, Nankai University, Tianjin, China
› Author Affiliations

Supported by: Key R&D Program of China 2021YFA1500200
Supported by: National Natural Science Foundation of China 22221002,22301145,92256301
Supported by: New Cornerstone Science Foundation
Supported by: 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.


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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.

Supplementary Material



Publication History

Received: 20 May 2025

Accepted after revision: 01 July 2025

Accepted Manuscript online:
01 July 2025

Article published online:
22 July 2025

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