Ruthenium-Catalysed Dehydrogenative C–H Borylation of Arenes with Pinacolborane

A ruthenium complex prepared in situ from [RuCl2(p-cymene)]2 and TpMe2K [TpMe2 = hydrotris(3,5-dimethylpyrazolyl)borate] is efficient for aromatic C–H borylation with pinacolborane (4,4,5,5-tetramethyl-1,3,2-dioxaborolane). Arenes were borylated at more electron-rich positions. DFT calculations and...

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Veröffentlicht in:Journal of chemical research 2016-07, Vol.40 (7), p.393-396
Hauptverfasser: Murata, Miki, Ueda, Yosuke, Hyogo, Mayu, Kohari, Yoshihito, Namikoshi, Takeshi, Watanabe, Shinji
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container_end_page 396
container_issue 7
container_start_page 393
container_title Journal of chemical research
container_volume 40
creator Murata, Miki
Ueda, Yosuke
Hyogo, Mayu
Kohari, Yoshihito
Namikoshi, Takeshi
Watanabe, Shinji
description A ruthenium complex prepared in situ from [RuCl2(p-cymene)]2 and TpMe2K [TpMe2 = hydrotris(3,5-dimethylpyrazolyl)borate] is efficient for aromatic C–H borylation with pinacolborane (4,4,5,5-tetramethyl-1,3,2-dioxaborolane). Arenes were borylated at more electron-rich positions. DFT calculations and kinetic isotope effect experiments suggest that the catalytic cycle should involve an electrophilic aromatic substitution with a borenium cation.
doi_str_mv 10.3184/174751916X14639973714726
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subjects Aromatic compounds
Catalysis
Cations
Dehydrogenation
Isotope effect
Mathematical analysis
Reaction kinetics
Ruthenium
title Ruthenium-Catalysed Dehydrogenative C–H Borylation of Arenes with Pinacolborane
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