Pd‐Catalyzed Cross‐Coupling of Organozinc Pivalates with Arene Thianthrenium Salts Under Ball‐Milling Conditions

Abstract Cross‐coupling reactions are important tools in the synthesis of complex molecules. In this work, we show that the Pd‐catalyzed cross‐coupling of aryl zinc pivalates with aryl thianthrenium salts offers a greener way to realize Negishi cross‐coupling reaction. Our results show that organozinc pivalates are air‐stable alternatives to classical organozinc halides and are suitable for mechanochemical reactions. Arene thianthrenium salts are alternative electrophilic reagents that are more compatible and selective than traditional organic halides. Moreover, the majority of thianthrene can be recovered after the cross‐coupling reaction.

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Publication Details

Journal
ChemCatChem
Published
2025-03-31
DOI
https://doi.org/10.1002/cctc.202500373
Citations
4
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
3.74
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article

Pd‐Catalyzed Cross‐Coupling of Organozinc Pivalates with Arene Thianthrenium Salts Under Ball‐Milling Conditions

Radovan Šebesta, Tomáš Čarný, Mehmet Mart, Michał Błauciak et al.
4 citations
ChemCatChem
Catalytic Cross-Coupling Reactions
3.74
article

Pd‐Catalyzed Cross‐Coupling of Organozinc Pivalates with Arene Thianthrenium Salts Under Ball‐Milling Conditions

Radovan Šebesta, Tomáš Čarný, Mehmet Mart, Michał Błauciak, Barbora Steinhüblová
article en
4 citations

Abstract

Abstract Cross‐coupling reactions are important tools in the synthesis of complex molecules. In this work, we show that the Pd‐catalyzed cross‐coupling of aryl zinc pivalates with aryl thianthrenium salts offers a greener way to realize Negishi cross‐coupling reaction. Our results show that organozinc pivalates are air‐stable alternatives to classical organozinc halides and are suitable for mechanochemical reactions. Arene thianthrenium salts are alternative electrophilic reagents that are more compatible and selective than traditional organic halides. Moreover, the majority of thianthrene can be recovered after the cross‐coupling reaction.

ChemCatChemVol. 17(11)
Wrocław University of Science and Technology (PL), Wroclaw University of Economics and Business (PL), AGH University of Krakow (PL), Comenius University Bratislava (SK)
Openalex Percentile: Top 8%
Catalytic Cross-Coupling Reactions
3.74
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