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.

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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
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Nickel-Catalyzed Carbonylative Synthesis of 1,6-Diketones from Cycloalkylsilyl Peroxides and Arylboronic Acids

Xiao‐Feng Wu, Jiacong Ma, Zilin Huang, Hongyi Huang et al.
Organic Letters
Catalytic Cross-Coupling Reactions
article

Nickel-Catalyzed Carbonylative Synthesis of 1,6-Diketones from Cycloalkylsilyl Peroxides and Arylboronic Acids

Xiao‐Feng Wu, Jiacong Ma, Zilin Huang, Hongyi Huang, Xinxin Qi
article en

Abstract

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.

Organic Letters
Zhejiang Sci-Tech University (CN), Chinese Academy of Engineering (CN), Leibniz Institute for Catalysis (DE), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 21%
Catalytic Cross-Coupling Reactions
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