Synlett
DOI: 10.1055/a-2726-4625
Synpacts

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

Authors

  • Canbin Qiu

    1   Center for Supramolecular and Catalytic Chemistry, Department of Chemistry, Shanghai University, Shanghai, China
  • Hegui Gong

    2   Institute of Nanoscience and Engineering, Henan University, Kaifeng, China (Ringgold ID: RIN12411)

We acknowledge the National Natural Science Foundation of China (22271182) for financial support.


Graphical 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.



Publication History

Received: 18 September 2025

Accepted: 17 October 2025

Accepted Manuscript online:
17 October 2025

Article published online:
19 November 2025

© 2025. Thieme. All rights reserved.

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany