Nickel-Catalyzed Carbonylative Synthesis of 1,6-Diketones from Cycloalkylsilyl Peroxides and Arylboronic Acids
Abstract A nickel catalyst has been successfully explored for the carbonylative synthesis of 1,6-diketones from cycloalkylsilyl peroxides and arylboronic acids. Under nickel catalysis, using cycloalkylsilyl peroxides as carbonyl-containing alkyl radicals and formic acid as a safe CO source, the protocol affords a variety of 1,6-diketones in good yields, in general with promising functional group tolerance. This transformation represents a general and complementary strategy for the construction of valuable 1,6-diketones.
Authors
- Xiao‐Feng Wu (ORCID: https://orcid.org/0000-0001-6622-3328)
- Jiacong Ma
- Zilin Huang (ORCID: https://orcid.org/0009-0003-7369-2917)
- Hongyi Huang
- Xinxin Qi
Institutions
- Zhejiang Sci-Tech University (CN)
- Chinese Academy of Engineering (CN)
- Leibniz Institute for Catalysis (DE)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-09-21
- DOI
- https://doi.org/10.1021/acs.orglett.6c03636
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00