Enantioselective Suzuki–Miyaura Coupling of Unactivated C–O Electrophiles via Nickel Catalysis

Herein, the first nickel-catalyzed enantioselective Suzuki-Miyaura coupling of unactivated C-O electrophiles is demonstrated and facilitates the preparation of valuable atropisomeric 2-hydroxybiaryls without the demand for highly reactive organometallic reagents. Furthermore, we conduct derivation experiments for the synthesis of diverse privileged chiral catalysts and ligands.

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Publication Details

Journal
Organic Letters
Published
2025-10-29
DOI
https://doi.org/10.1021/acs.orglett.5c04110
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
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article

Enantioselective Suzuki–Miyaura Coupling of Unactivated C–O Electrophiles via Nickel Catalysis

Zhi‐Chao Cao, Kun Liu, Linchao Guo, Yusheng Su
Organic Letters
Axial and Atropisomeric Chirality Synthesis
article

Enantioselective Suzuki–Miyaura Coupling of Unactivated C–O Electrophiles via Nickel Catalysis

Zhi‐Chao Cao, Kun Liu, Linchao Guo, Yusheng Su
article en

Abstract

Herein, the first nickel-catalyzed enantioselective Suzuki-Miyaura coupling of unactivated C-O electrophiles is demonstrated and facilitates the preparation of valuable atropisomeric 2-hydroxybiaryls without the demand for highly reactive organometallic reagents. Furthermore, we conduct derivation experiments for the synthesis of diverse privileged chiral catalysts and ligands.

Organic LettersVol. 27(44)
Anhui Agricultural University (CN)
Openalex Percentile: Top 76%
Axial and Atropisomeric Chirality Synthesis
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