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Metal‐Free C−H Borylation of N‐Heteroarenes by Boron Trifluoride

Vladimir Iashin, Dénes Berta, Konstantin Chernichenko, Martin Nieger, Karina Moslova, Imre Pápai, Timo Repo

2020Chemistry - A European Journal28 citationsDOIOpen Access PDF

Abstract

Abstract Organoboron compounds are essential reagents in modern C−C coupling reactions. Their synthesis via catalytic C−H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal‐free synthesis of aryldifluoroboranes from BF 3 and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.

Topics & Concepts

BorylationBoron trifluorideBoronMetalChemistryOrganic chemistryCatalysisArylAlkylOrganoboron and organosilicon chemistryCatalytic C–H Functionalization MethodsBoron Compounds in Chemistry
Metal‐Free C−H Borylation of N‐Heteroarenes by Boron Trifluoride | Litcius