Arene borylation reactions provide direct access to aryl organoboranes, including aryl boronic esters. Precious metals, namely Ir, Rh, Pt, remain the go-to for metal-catalysed borylation reactions, however, significant efforts have been expended in developing Earth-abundant metal alternatives. The iron-catalysed borylation of 2-aryl pyridine derivatives with 9-borabicyclo[3.3.1]nonane (H-B-9-BBN) offers unique reactivity by using only FeBr as the catalyst, without added ligand(s). Mechanistic analysis of this borylation reaction revealed an alternative, hidden catalysis pathway whereby the iron salt acts not as a borylation catalyst, but as an initiator for the generation of a catalytically active haloborane, Br-B-9-BBN. The roles of iron salt, Br-B-9-BBN, and HBr in catalyst formation, the mode of catalytic turnover, and catalyst regeneration were all determined using single-turnover and catalytic studies. The borylation reaction was found to proceed by a catalytic electrophilic borylation using, in situ generated, Br-B-9-BBN. These studies highlight a new, orthogonal method of generating haloboranes and their previously unobserved role as hidden catalysts within arene borylation reactions.
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http://dx.doi.org/10.1002/anie.202423929 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh, David Brewster Road. Edinburgh, EH9 3FJ, UK.
Org Lett
December 2024
Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
Arylborane complexes ligated by N-heterocyclic carbenes (NHCs) can be synthesized by photoirradiation of a mixture of NHC-boranes and sulfonyl(hetero)arenes. The reaction occurs under mild and convenient conditions without any photocatalyst, which are realized by a radical chain mechanism involving NHC-boryl radicals and sulfonyl radicals. This reaction offered the opportunity to reveal the photophysical property of a 2-borylnaphtho[1,2-]thiazole derivative.
View Article and Find Full Text PDFOrg Lett
December 2024
Department of Chemistry, The University of Texas at Austin, 100 East 24th Street, Austin, Texas 78712, United States.
Herein, we report the palladium-catalyzed borylation of aryl halides (iodides or bromides) under base-free conditions utilizing a commercially available Lewis acidic mediator, Zn(OTf). Under these conditions, an array of electronically and functional-group-diverse aryl iodides and bromides undergo borylation to afford the corresponding aryl boronic esters in ≤82% isolated yields. Mechanistic investigations are consistent with Zn(OTf) enabling transmetalation between a cationic Pd(II)-Ar intermediate and Bpin via halide abstraction.
View Article and Find Full Text PDFNat Commun
November 2024
College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.
Aryl thianthrenium salts are valuable in photocatalysis but traditionally require external electron donors for activation. This study introduces an energy transfer (EnT) strategy for the activation of aryl thianthrenium salts using 2,3,4,5,6-penta(carbazol-9-yl)benzonitrile (5CzBN) as a metal-free photocatalyst, eliminating the need for external donors. Utilizing this EnT approach, we achieve C-H deuteration of arenes under visible light with CDCl as a deuterium source to synthesize various deuterated aromatic compounds, including important natural products and pharmaceuticals.
View Article and Find Full Text PDFJACS Au
September 2024
Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
Site-selective C-H borylation is an important strategy for constructing molecular diversity in arenes and heteroarenes. Although transition-metal-catalyzed borylation is well explored, developing metal-free strategies remains scarce. Herein, we developed a straightforward approach for BBr-mediated selective C-H borylation of naphthamide and phenyl acetamide derivatives under metal-free conditions.
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