Electrochemical SynergisticNi/Co-Catalyzed CarbonylativeCross-Electrophile Coupling of Aryl and Alkyl Halides with CO

Accessing unsymmetric ketones and achieving their carbon isotope labeling are crucial yet challenging tasks in both synthetic and medicinal chemistry. We report here an efficient electrochemical nickel-/cobalt-catalyzed carbonylative cross-electrophile coupling reaction. This method allows for the modular synthesis of a library of unsymmetric ketones from simple building blocks, including aryl halides, alkyl halides, and gaseous CO. The simultaneous use of nickel and cobalt salts as concerted catalysts ensures the high efficiency of this three-component carbonylative coupling. Furthermore, electrochemical reduction avoids the use of stoichiometric reductants, making this protocol more sustainable and attractive. The broad substrate scope and late-stage <sup>13</sup>C isotope labeling of complex molecules derived from biologically active compounds highlight the practicality of this method.

Publication Details

Journal
Figshare
Published
2025-03-05
DOI
https://doi.org/10.1021/jacsau.5c00031.s001
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electrochemical SynergisticNi/Co-Catalyzed CarbonylativeCross-Electrophile Coupling of Aryl and Alkyl Halides with CO

Figshare
Chemical Reactions and Isotopes
article

Electrochemical SynergisticNi/Co-Catalyzed CarbonylativeCross-Electrophile Coupling of Aryl and Alkyl Halides with CO

article en

Abstract

Accessing unsymmetric ketones and achieving their carbon isotope labeling are crucial yet challenging tasks in both synthetic and medicinal chemistry. We report here an efficient electrochemical nickel-/cobalt-catalyzed carbonylative cross-electrophile coupling reaction. This method allows for the modular synthesis of a library of unsymmetric ketones from simple building blocks, including aryl halides, alkyl halides, and gaseous CO. The simultaneous use of nickel and cobalt salts as concerted catalysts ensures the high efficiency of this three-component carbonylative coupling. Furthermore, electrochemical reduction avoids the use of stoichiometric reductants, making this protocol more sustainable and attractive. The broad substrate scope and late-stage <sup>13</sup>C isotope labeling of complex molecules derived from biologically active compounds highlight the practicality of this method.

Figshare
Responsible consumption and production
Openalex Percentile: Top 65%
Chemical Reactions and Isotopes
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.