Aryl Boronic Esters Are Stable on Silica Gel and Reactive under Suzuki–Miyaura Coupling Conditions

A wide range of aryl boronic 1,1,2,2-tetraethylethylene glycol esters [ArB­(Epin)­s] were readily synthesized. Purifying aryl boronic esters by conventional silica gel chromatography is generally challenging; however, these introduced derivatives are easily purified on silica gel and isolated in exc...

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Veröffentlicht in:Organic letters 2022-05, Vol.24 (19), p.3510-3514
Hauptverfasser: Oka, Naoki, Yamada, Tsuyoshi, Sajiki, Hironao, Akai, Shuji, Ikawa, Takashi
Format: Artikel
Sprache:eng
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Zusammenfassung:A wide range of aryl boronic 1,1,2,2-tetraethylethylene glycol esters [ArB­(Epin)­s] were readily synthesized. Purifying aryl boronic esters by conventional silica gel chromatography is generally challenging; however, these introduced derivatives are easily purified on silica gel and isolated in excellent yields. We subjected the purified ArB­(Epin) to Suzuki–Miyaura couplings, which provided higher yields of the desired biaryl products than those obtained using the corresponding aryl boronic acids or pinacol esters.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c01174