Iron‐Catalysed Borylation of Arenediazonium Salts to Give Access to Arylboron Derivatives via Aryl(amino)boranes at Room Temperature
Ludovic D. Marciasini, Nicolas Richy, Michel Vaultier, Mathieu Pucheault
Abstract
Ludovic D. Marciasini, Nicolas Richy, Michel Vaultier, Mathieu Pucheault
Abstract
Abstract Complementary to previously described Miyaura borylation methods, a new access to boron derivatives via aryl(amino)boranes is described. Direct coupling between aryldiazonium salts and diisopropylaminoborane is catalysed by 0.1% ferrocene leading to the formation of a carbon‐boron bond. The obtained aryl(amino)boranes could eventually then be transformed into boronic acids, boronates or borates.
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Abstract Complementary to previously described Miyaura borylation methods, a new access to boron derivatives via aryl(amino)boranes is described. Direct coupling between aryldiazonium salts and diisopropylaminoborane is catalysed by 0.1% ferrocene leading to the formation of a carbon‐boron bond. The obtained aryl(amino)boranes could eventually then be transformed into boronic acids, boronates or borates.
Key concepts: Borylation, Boranes, Chemistry, Aryl, Boron, Ferrocene, Organic chemistry, Combinatorial chemistry