Preparation of Chiral α-Aryl Ketones and Aldehydes via Ni-Catalyzed Asymmetric Cross-Electrophile Coupling

Abstract The preparation of tertiary α-aryl acetals and ketals has been achieved through a Ni-catalyzed reductive cross-coupling approach, utilizing a readily available Ni/Biox catalytic platform. This reaction demonstrates effective enantioselective control over unactivated alkyl radicals adjacent to sterically bulky acetal and ketal groups. The resulting protected tertiary α-aryl ketones and aldehydes are configurationally stable, offering opportunities for further chemical manipulations.

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Publication Details

Journal
Synlett
Published
2025-10-17
DOI
https://doi.org/10.1055/a-2726-4625
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Preparation of Chiral α-Aryl Ketones and Aldehydes via Ni-Catalyzed Asymmetric Cross-Electrophile Coupling

Hegui Gong, Canbin Qiu
Synlett
Catalytic C–H Functionalization Methods
article

Preparation of Chiral α-Aryl Ketones and Aldehydes via Ni-Catalyzed Asymmetric Cross-Electrophile Coupling

Hegui Gong, Canbin Qiu
article en

Abstract

Abstract The preparation of tertiary α-aryl acetals and ketals has been achieved through a Ni-catalyzed reductive cross-coupling approach, utilizing a readily available Ni/Biox catalytic platform. This reaction demonstrates effective enantioselective control over unactivated alkyl radicals adjacent to sterically bulky acetal and ketal groups. The resulting protected tertiary α-aryl ketones and aldehydes are configurationally stable, offering opportunities for further chemical manipulations.

SynlettVol. 37(04)
University of Shanghai for Science and Technology (CN), Henan University (CN), Catalytic Materials (United States) (US)
Openalex Percentile: Top 78%
Catalytic C–H Functionalization Methods
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