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.
Authors
- Hegui Gong (ORCID: https://orcid.org/0000-0001-6534-5569)
- Canbin Qiu (ORCID: https://orcid.org/0000-0002-6738-2782)
Institutions
- University of Shanghai for Science and Technology (CN)
- Henan University (CN)
- Catalytic Materials (United States) (US)
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
- Field-Weighted Citation Impact
- 0.00